US20190194516A1 - Automotive engine coolant composition, automotive engine concentrated coolant composition, and method of operating internal combustion engine - Google Patents
Automotive engine coolant composition, automotive engine concentrated coolant composition, and method of operating internal combustion engine Download PDFInfo
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- US20190194516A1 US20190194516A1 US16/311,986 US201716311986A US2019194516A1 US 20190194516 A1 US20190194516 A1 US 20190194516A1 US 201716311986 A US201716311986 A US 201716311986A US 2019194516 A1 US2019194516 A1 US 2019194516A1
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- coolant composition
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- rubber
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- 239000002826 coolant Substances 0.000 title claims abstract description 170
- 239000000203 mixture Substances 0.000 title claims abstract description 143
- 238000000034 method Methods 0.000 title claims description 14
- 238000002485 combustion reaction Methods 0.000 title claims description 12
- 229920001971 elastomer Polymers 0.000 claims abstract description 91
- 239000005060 rubber Substances 0.000 claims abstract description 91
- -1 glycol monoalkyl ether Chemical class 0.000 claims abstract description 79
- 239000003112 inhibitor Substances 0.000 claims abstract description 69
- 230000008961 swelling Effects 0.000 claims abstract description 67
- 239000004094 surface-active agent Substances 0.000 claims abstract description 48
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims abstract description 40
- 150000001875 compounds Chemical class 0.000 claims abstract description 33
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- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 25
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 13
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 11
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 9
- 239000001257 hydrogen Substances 0.000 claims abstract description 9
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims abstract description 9
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- 239000003960 organic solvent Substances 0.000 claims description 9
- 239000002904 solvent Substances 0.000 claims description 7
- 239000002585 base Substances 0.000 description 33
- 229910052783 alkali metal Inorganic materials 0.000 description 31
- 150000001339 alkali metal compounds Chemical class 0.000 description 26
- 230000000694 effects Effects 0.000 description 23
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- 239000000654 additive Substances 0.000 description 17
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- 238000001816 cooling Methods 0.000 description 12
- AKEJUJNQAAGONA-UHFFFAOYSA-N sulfur trioxide Inorganic materials O=S(=O)=O AKEJUJNQAAGONA-UHFFFAOYSA-N 0.000 description 11
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- 239000000446 fuel Substances 0.000 description 5
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 5
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- 125000003827 glycol group Chemical group 0.000 description 4
- FBSFWRHWHYMIOG-UHFFFAOYSA-N methyl 3,4,5-trihydroxybenzoate Chemical compound COC(=O)C1=CC(O)=C(O)C(O)=C1 FBSFWRHWHYMIOG-UHFFFAOYSA-N 0.000 description 4
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
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- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- KDVYCTOWXSLNNI-UHFFFAOYSA-N 4-t-Butylbenzoic acid Chemical compound CC(C)(C)C1=CC=C(C(O)=O)C=C1 KDVYCTOWXSLNNI-UHFFFAOYSA-N 0.000 description 1
- UJRRFYOOIAUSJA-UHFFFAOYSA-N 5-methylheptane-1,2,4-triol Chemical compound CCC(C)C(O)CC(O)CO UJRRFYOOIAUSJA-UHFFFAOYSA-N 0.000 description 1
- BSYNRYMUTXBXSQ-FOQJRBATSA-N 59096-14-9 Chemical compound CC(=O)OC1=CC=CC=C1[14C](O)=O BSYNRYMUTXBXSQ-FOQJRBATSA-N 0.000 description 1
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- APMBKEPKBIUABM-UHFFFAOYSA-N CC(C)(C)C1=C(O)C=CC(O)=C1.CC(C)(C)C1=CC(O)=C(O)C=C1.COC(=O)C1=CC(O)=C(O)C(O)=C1.COC(=O)C1=CC(O)=CC(O)=C1.COC1=CC=C(O)C=C1.O=C(O)CCSSCCC(=O)O Chemical compound CC(C)(C)C1=C(O)C=CC(O)=C1.CC(C)(C)C1=CC(O)=C(O)C=C1.COC(=O)C1=CC(O)=C(O)C(O)=C1.COC(=O)C1=CC(O)=CC(O)=C1.COC1=CC=C(O)C=C1.O=C(O)CCSSCCC(=O)O APMBKEPKBIUABM-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- ODBLHEXUDAPZAU-ZAFYKAAXSA-N D-threo-isocitric acid Chemical compound OC(=O)[C@H](O)[C@@H](C(O)=O)CC(O)=O ODBLHEXUDAPZAU-ZAFYKAAXSA-N 0.000 description 1
- ODBLHEXUDAPZAU-FONMRSAGSA-N Isocitric acid Natural products OC(=O)[C@@H](O)[C@H](C(O)=O)CC(O)=O ODBLHEXUDAPZAU-FONMRSAGSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- 229920001214 Polysorbate 60 Polymers 0.000 description 1
- 239000004111 Potassium silicate Substances 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- 239000005708 Sodium hypochlorite Substances 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- AZFNGPAYDKGCRB-XCPIVNJJSA-M [(1s,2s)-2-amino-1,2-diphenylethyl]-(4-methylphenyl)sulfonylazanide;chlororuthenium(1+);1-methyl-4-propan-2-ylbenzene Chemical compound [Ru+]Cl.CC(C)C1=CC=C(C)C=C1.C1=CC(C)=CC=C1S(=O)(=O)[N-][C@@H](C=1C=CC=CC=1)[C@@H](N)C1=CC=CC=C1 AZFNGPAYDKGCRB-XCPIVNJJSA-M 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 125000003282 alkyl amino group Chemical group 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 150000001983 dialkylethers Chemical class 0.000 description 1
- 229940028356 diethylene glycol monobutyl ether Drugs 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 1
- AHMROPIAMLLAPW-UHFFFAOYSA-L dipotassium;decanedioate Chemical compound [K+].[K+].[O-]C(=O)CCCCCCCCC([O-])=O AHMROPIAMLLAPW-UHFFFAOYSA-L 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- TUEYHEWXYWCDHA-UHFFFAOYSA-N ethyl 5-methylthiadiazole-4-carboxylate Chemical compound CCOC(=O)C=1N=NSC=1C TUEYHEWXYWCDHA-UHFFFAOYSA-N 0.000 description 1
- 229920001973 fluoroelastomer Polymers 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 229940074391 gallic acid Drugs 0.000 description 1
- 235000004515 gallic acid Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229940051250 hexylene glycol Drugs 0.000 description 1
- 125000001165 hydrophobic group Chemical group 0.000 description 1
- 150000002440 hydroxy compounds Chemical class 0.000 description 1
- QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- VLAPMBHFAWRUQP-UHFFFAOYSA-L molybdic acid Chemical compound O[Mo](O)(=O)=O VLAPMBHFAWRUQP-UHFFFAOYSA-L 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 238000013021 overheating Methods 0.000 description 1
- JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 description 1
- 239000002530 phenolic antioxidant Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229940051841 polyoxyethylene ether Drugs 0.000 description 1
- 229920000056 polyoxyethylene ether Polymers 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- SATVIFGJTRRDQU-UHFFFAOYSA-N potassium hypochlorite Chemical compound [K+].Cl[O-] SATVIFGJTRRDQU-UHFFFAOYSA-N 0.000 description 1
- 235000010333 potassium nitrate Nutrition 0.000 description 1
- 239000004323 potassium nitrate Substances 0.000 description 1
- 235000010289 potassium nitrite Nutrition 0.000 description 1
- 239000004304 potassium nitrite Substances 0.000 description 1
- 229910000160 potassium phosphate Inorganic materials 0.000 description 1
- 235000011009 potassium phosphates Nutrition 0.000 description 1
- NNHHDJVEYQHLHG-UHFFFAOYSA-N potassium silicate Chemical compound [K+].[K+].[O-][Si]([O-])=O NNHHDJVEYQHLHG-UHFFFAOYSA-N 0.000 description 1
- 229910052913 potassium silicate Inorganic materials 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 1
- 229910052939 potassium sulfate Inorganic materials 0.000 description 1
- 235000011151 potassium sulphates Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
- 239000011684 sodium molybdate Substances 0.000 description 1
- 235000015393 sodium molybdate Nutrition 0.000 description 1
- TVXXNOYZHKPKGW-UHFFFAOYSA-N sodium molybdate (anhydrous) Chemical compound [Na+].[Na+].[O-][Mo]([O-])(=O)=O TVXXNOYZHKPKGW-UHFFFAOYSA-N 0.000 description 1
- 239000004317 sodium nitrate Substances 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 230000019635 sulfation Effects 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- ODBLHEXUDAPZAU-UHFFFAOYSA-N threo-D-isocitric acid Natural products OC(=O)C(O)C(C(O)=O)CC(O)=O ODBLHEXUDAPZAU-UHFFFAOYSA-N 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- WUUHFRRPHJEEKV-UHFFFAOYSA-N tripotassium borate Chemical compound [K+].[K+].[K+].[O-]B([O-])[O-] WUUHFRRPHJEEKV-UHFFFAOYSA-N 0.000 description 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K5/00—Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
- C09K5/08—Materials not undergoing a change of physical state when used
- C09K5/10—Liquid materials
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K5/00—Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
- C09K5/20—Antifreeze additives therefor, e.g. for radiator liquids
Definitions
- the present invention relates to an automotive engine coolant composition, an automotive engine concentrated coolant composition, and a method of operating an internal combustion engine.
- coolant for cooling automotive engines and the like Various types of coolant for cooling automotive engines and the like are known, and among the coolants, water has been widely used as engine coolant because of its highest cooling performance.
- pure water which does not contain an electrolyte and the like, freezes at 0° C. or lower, and increases in volume, possibly leading to damage to the engine and radiator. Therefore, a coolant composition, which does not use only pure water, and is formed by using a glycol such as ethylene glycol as the base for the purpose of antifreeze properties, diluting this with water so as to obtain a required freezing temperature, and mixing various additives for protecting metals, rubbers, resins, and the like used in the engine or radiator from deterioration as necessary therein has been used.
- a viscosity index improver is mixed therein (Japanese Patent No. 5904278), and a technique for prompting quick warm-up of the engine and improving fuel efficiency by mixing a surfactant as a viscosity index improver in a coolant and thus appropriately increasing viscosity has been carried out.
- the surfactant since the surfactant has the drawback of swelling the rubber used in automotive parts, an antioxidant has been blended in order to suppress the volume change of the rubber under the immersion environment in the coolant.
- JP 2009-242663 A Japanese Patent Application Publication No. 2009-242663
- a sulfur-containing alcohol or a phenol-based antioxidant is mixed in a rubber swelling antifreeze/coolant composition containing an aliphatic monobasic acid.
- WO2004/050785 it is described that hydroxybenzoic acid, isocitric acid, acetylsalicylic acid, and the like are mixed as additives for improving the thermal stability of glycol components.
- the coolant mixed with the antioxidant as described above has a possibility that there may be insufficient effect in suppressing swelling of rubber or the coolant may be significantly discolored.
- the present invention provides an automotive engine coolant composition which has a specific kinematic viscosity and is capable of suppressing swelling of contacting rubber and discoloration of a coolant.
- the present invention also provides an automotive engine concentrated coolant composition for obtaining such an automotive engine coolant composition.
- the inventors completed the present invention by combining a coolant composition containing a surfactant and a base with a specific rubber swelling inhibitor in a specific amount.
- the present invention includes the following inventions.
- An automotive engine coolant composition including: a surfactant as a viscosity index improver; a rubber swelling inhibitor; and a base, in which
- the rubber swelling inhibitor is at least one selected from a compound expressed by a following formula (1):
- R 1 is hydrogen, a methyl group, or an ethyl group
- the base includes at least one alcohol selected from the group consisting of a monohydric alcohol, a dihydric alcohol, a trihydric alcohol, and a glycol monoalkyl ether and/or water and has a kinematic viscosity of 8.5 mm 2 /s or more at 25° C., and a content of the rubber swelling inhibitor is 0.03 parts by mass or more and 0.9 parts by mass or less with respect to 100 parts by mass of the coolant composition.
- the coolant composition according to [1] or [2], in which the content of the rubber swelling inhibitor may be 0.05 parts by mass or more and 0.5 parts by mass or less with respect to 100 parts by mass of the coolant composition.
- a content of the surfactant may be 0.005 parts by mass or more and 3 parts by mass or less with respect to 100 parts by mass of the coolant composition.
- An automotive engine concentrated coolant composition for obtaining the coolant composition according to any one of [1] to [6], which is diluted 2 to 10 times by mass with a base so as to be used.
- the automotive engine coolant composition of the present invention has a specific kinematic viscosity and thus can improve the fuel efficiency effect of an internal combustion engine.
- the automotive engine coolant composition of the present invention can suppress swelling of rubber used in automotive parts while suppressing discoloration of the coolant.
- the automotive engine coolant composition can be obtained by diluting the automotive engine concentrated coolant composition of the present invention.
- FIG. 1A is a diagram showing a putative mechanism for swelling of rubber
- FIG. 1B is a diagram showing a putative mechanism for swelling of rubber
- FIG. 1C is a diagram showing a putative mechanism for swelling of rubber
- FIG. 1D is a diagram showing a putative mechanism for swelling of rubber.
- FIG. 1E is a diagram showing a putative mechanism for swelling of rubber.
- An automotive engine coolant composition of the present invention (hereinafter, also referred to as a coolant composition of the present invention) includes a surfactant (A) as a viscosity index improver, a specific rubber swelling inhibitor (B), and a base (C).
- a surfactant A
- B a specific rubber swelling inhibitor
- C a base
- the inventors found that by combining a coolant composition containing a surfactant as a viscosity index improver and a base with a specific rubber swelling inhibitor, a specific kinematic viscosity is imparted due to an appropriate thickening effect exhibited by the surfactant, and it becomes possible to suppress swelling of contacting rubber and discoloration of the coolant.
- a coolant mixed with an antioxidant of the related art, particularly a phenolic antioxidant is not effective enough to suppress swelling of rubber and causes significant discoloration.
- the coolant composition of the present invention mixed with the specific rubber swelling inhibitor (B) is excellent both in suppression of swelling of rubber and suppression of discoloration.
- the rubber swelling inhibitor (B) suppresses oxidation deterioration due to oxygen brought into rubber by the surfactant such that it becomes possible to suppress swelling of rubber.
- a putative mechanism for swelling of rubber in a coolant mixed with a surfactant is illustrated in FIGS. 1A to 1E .
- a hydrophobic group of the surfactant as a viscosity index improver penetrates into the rubber contacting the coolant ( FIGS. 1A and 1B ), and a hydrophilic group of the surfactant brings the coolant in which oxygen is dissolved into the rubber such that the rubber is swelled ( FIG. 1C ).
- Oxygen brought into the rubber oxidizes and deteriorates the rubber and the cross-link density of the rubber decreases due to breaking of the molecular chain and introduction of oxygen atoms into the molecule ( FIG. 1D ).
- the surfactant and the coolant in which oxygen is dissolved are further brought into and penetrate into the dense rubber surface layer, and the rubber is swelled ( FIG. 1E ).
- the penetrated oxygen further oxidized and deteriorated the rubber, and the surfactant further brings the coolant in which oxygen is dissolved into the rubber, resulting in an increase in the swelling of the rubber ( FIG. 1E ).
- the term “rubber” refers to those that are in contact with an automotive engine coolant, such as an automotive engine, an inverter, a battery, and hoses. Specific examples thereof include ethylene propylene diene rubber (EPDM), hydrogenated nitrile rubber (H-NBR), nitrile rubber (NBR), fluoro rubber (FKM), and silicone rubber (VMQ).
- EPDM ethylene propylene diene rubber
- H-NBR hydrogenated nitrile rubber
- NBR nitrile rubber
- FKM fluoro rubber
- silicone rubber silicone rubber
- a “low temperature” means, for example, 25° C. and a “high temperature” means, for example, 100° C.
- the surfactant (A) used in the coolant composition of the present invention can be typically used as a viscosity index improver in the coolant composition and is not particularly limited as long as the effects of the present invention can be obtained.
- the surfactant (A) may be any of a nonionic surfactant, an anionic surfactant, a cationic surfactant, and an amphoteric surfactant.
- One type of the surfactant (A) may be used singly, or two or more types thereof may be used in combination.
- nonionic surfactant examples include a compound having a polyalkylene glycol chain, an ester of a fatty acid with a polyhydric alcohol such as glycerin, sorbitol, or sucrose, a fatty acid alkanolamide, and the like. From the viewpoint of heat resistance and water solubility, a compound having a polyalkylene glycol chain is preferable, and a compound having a polyethylene glycol chain is more preferable.
- Examples of the compound having a polyethylene glycol chain include polyoxyethylene polyoxypropylene glycol, polyoxyethylene monoalkyl ether, polyoxyethylene dialkyl ether, polyoxyethylene polyoxypropylene alkyl ether, polyoxyethylene alkyl phenyl ether, polyethylene glycol polyhydric alcohol ether, polyethylene glycol alkyl amino ether, polyethylene glycol mono fatty acid ester, polyethylene glycol difatty acid ester, polyoxyethylene sorbitan fatty acid ester, polyoxyethylene sorbitol fatty acid ester, polyoxyethylene glycerin fatty acid ester, polyoxyethylene castor oil, polyoxyethylene hydrogenated castor oil, and polyoxyethylene fatty acid amide.
- polyoxyethylene monoalkyl ether fatty acid alkanol amide, polyethylene glycol difatty acid ester, and polyoxyethylene fatty acid amide, which greatly increase in kinematic viscosity at 25° C. and slightly increase in kinematic viscosity at 100° C. in a low mixing amount, are preferable, and polyoxyethylene monoalkyl ether is more preferable.
- the polyoxyalkylene alkyl ether is preferably a compound represented by the following formula (3):
- R a is a linear or branched alkyl or alkenyl group having 12 or more and 24 or less carbon atoms
- R b is an ethylene group or a propylene group
- p represents an average number of moles of R b O added, and is a number from 0.5 or more and 20 or less.
- the alkyl group or alkenyl group may be linear or branched, and is preferably linear from the viewpoint of thickening effect.
- the number of carbon atoms of the alkyl group or alkenyl group is preferably 12 or more and 24 or less, more preferably 16 or more and 22 or less, and even more preferably 20 or more and 22 or less.
- an alkyl group such as a lauryl group, a myristyl group, a cetyl group, a margaryl group, an isostearyl group, a 2-heptylundecyl group, a stearyl group, an arachidyl group, a behenyl group, and a lignoceryl group; and an alkenyl group such as an oleyl group.
- an alkyl group such as a lauryl group, a myristyl group, a cetyl group, a margaryl group, an isostearyl group, a 2-heptylundecyl group, a stearyl group, an arachidyl group, a behenyl group, and a lignoceryl group
- an alkenyl group such as an oleyl group.
- a cetyl group, a stearyl group, and a behenyl group are preferable, and a
- R b mentioned above is preferably an ethylene group or a propylene group, and is more preferably an ethylene group from the viewpoint of thickening effect.
- p mentioned above represents the average number of moles of R b O added, and from the viewpoint of thickening effect, is preferably a number from 0.5 or more and 20 or less, more preferably a number from 1 or more and 15 or less, even more preferably a number from 2 or more and 11 or less, and even more preferably a number from 3 or more and 8 or less.
- anionic surfactant examples include an alkyl sulfuric acid ester salt, a polyoxyethylene alkyl ether sulfuric acid ester salt, an alkylbenzene sulfonic acid salt, a fatty acid salt, an alkyl phosphoric acid ester salt, and a polyoxyethylene alkyl ether phosphoric acid ester salt.
- a polyoxyethylene alkyl ether sulfuric acid ester salt which greatly increases in kinematic viscosity at 25° C. and slightly increases in kinematic viscosity at 100° C. in a low mixing amount, is preferable.
- the polyoxyethylene alkyl ether sulfuric acid ester salt is preferably a compound represented by the following formula (4):
- R c is a linear or branched alkyl or alkenyl group having 16 or more and 24 or less carbon atoms
- R d is an ethylene group or a propylene group
- q represents an average number of moles of R d O added, and is a number from 0.5 or more and 10 or less
- M is a cation or a hydrogen atom.
- the alkyl group may be linear or branched, and is preferably linear from the viewpoint of thickening effect.
- the number of carbon atoms of the alkyl group and the alkenyl group is preferably 16 or more and 24 or less, more preferably 18 or more and 22 or less, and even more preferably 20 or more and 22 or less.
- an alkyl group such as a cetyl group, a margaryl group, an isostearyl group, a 2-heptylundecyl group, a stearyl group, an arachidyl group, a behenyl group, a lignoceryl group; and an alkenyl group such as an oleyl group.
- a cetyl group, a stearyl group, an arachidyl group, and a behenyl group are preferable, and a behenyl group is more preferable.
- R d mentioned above is preferably an ethylene group or a propylene group, and is more preferably an ethylene group from the viewpoint of thickening effect.
- q mentioned above represents the average number of moles of R d O added, and from the viewpoint of having a specific kinematic viscosity at a low temperature and a high temperature, is preferably a number from 0.5 or more and 10 or less, and more preferably a number from 1 or more and 8 or less, even more preferably a number from 2 or more and 7 or less, and even more preferably a number from 3 or more and 6 or less.
- M mentioned above is a cation or a hydrogen atom, and is preferably a cation.
- Specific examples of the cation include an alkali metal ion and an ammonium ion, and examples of the alkali metal include lithium, sodium, and potassium. Sodium or potassium is preferable.
- Examples of the cationic surfactant include an alkylamine salt and a quaternary ammonium salt.
- amphoteric surfactant examples include an alkylbetaine and an alkylamine oxide.
- the surfactant (A) used in the coolant composition of the present invention can be typically used as a viscosity index improver in the coolant composition and is not particularly limited as long as the effects of the present invention can be obtained. From the viewpoint of thickening effect, a nonionic surfactant or an anionic surfactant is preferable, and an anionic surfactant is more preferable.
- the coolant composition of the present invention may contain an alkali metal compound (A′).
- the surfactant (A) used is an anionic surfactant, particularly an anionic surfactant represented by the formula (4), the alkali metal compound (A′) is preferably contained.
- the alkali metal compound (A′) is at least one type selected from the group consisting of an alkali metal salt and an alkali metal hydroxide, and the alkali metal salt excludes the surfactant (A).
- the alkali metal include sodium, potassium, and lithium.
- the alkali metal salt include an alkali metal salt of an inorganic acid or an organic acid, and an alkali metal salt of a triazole or a thiazole.
- alkali metal salt of an inorganic acid examples include an alkali metal salt of nitrous acid such as sodium nitrite and potassium nitrite; an alkali metal salt of nitric acid such as sodium nitrate and potassium nitrate; an alkali metal salt of molybdic acid such as sodium molybdate and potassium molybdate; an alkali metal salt of hypochlorous acid such as sodium hypochlorite and potassium hypochlorite; an alkali metal salt of sulfuric acid such as sodium sulfate and potassium sulfate; an alkali metal salts of carbonic acid such as sodium carbonate and potassium carbonate; an alkali metal salt of hydrochloric acid such as sodium chloride and potassium chloride; an alkali metal salt of phosphoric acid such as sodium phosphate and potassium phosphate; an alkali metal salt of silicic acid such as sodium silicate and potassium silicate; and an alkali metal salt of boric acid such as sodium borate and potassium borate.
- alkali metal salt of an organic acid examples include an alkali metal salt of an aromatic carboxylic acid such as benzoic acid, p-toluic acid, and p-tertbutylbenzoic acid; and an alkali metal salt of an aliphatic polyvalent carboxylic acid such as azelaic acid, sebacic acid, undecanedioic acid, dodecanedioic acid, and citric acid.
- alkali metal salt of a triazole or a thiazole examples include an alkali metal salt of benzotriazole.
- an alkali metal salt of an aliphatic polyvalent carboxylic acid is preferable from the viewpoint of causing the kinematic viscosity of the coolant composition at a low temperature and a high temperature to be in the predetermined range described above, and dipotassium sebacate is more preferable.
- an alkali metal salt is used as a rust inhibitor and/or a pH adjusting agent, it is presumed that this is used as the alkali metal salt. In that case, an alkali metal compound does not necessarily need to be separately added.
- the alkali metal hydroxide is not particularly limited, and specific examples thereof include lithium hydroxide, sodium hydroxide, and potassium hydroxide.
- potassium hydroxide is preferable from the viewpoint of causing the kinematic viscosity of the coolant composition at a low temperature and a high temperature to be in the predetermined range described above.
- the content of the surfactant (A) in the coolant composition of the present invention is, with respect to the base described above (with respect to 100 g), preferably 0.01 mmol or more, more preferably 0.05 mmol or more, even more preferably 0.1 mmol or more, even more preferably 0.15 mmol or more, even more preferably 0.2 mmol or more, even more preferably 0.25 mmol or more, even more preferably 0.3 mmol or more, and even more preferably 0.4 mmol or more from the viewpoint of causing the kinematic viscosity of the coolant composition at a low temperature and a high temperature to be in the predetermined range described above, is preferably 3 mmol or less, more preferably 2 mmol or less, even more preferably 1 mmol or less, and even more preferably 0.8 mmol or less from the viewpoint of enhancing cooling properties and suppressing semisolidification, and is preferably 0.01 mmol or more and 3 mmol or less, more preferably 0.05 mmol
- the content of the surfactant (A) is preferably in the range described above with respect to the total amount of the base and the rust inhibitor and/or the pH adjusting agent (with respect to 100 g).
- the content of the surfactant (A) in 100 parts by mass of the coolant composition of the present invention is preferably 0.005 parts by mass or more, more preferably 0.01 parts by mass or more, even more preferably 0.05 parts by mass or more, even more preferably 0.08 parts by mass or more, even more preferably 0.1 parts by mass or more, and even more preferably 0.2 parts by mass or more from the viewpoint of causing the kinematic viscosity of the coolant composition at a low temperature and a high temperature to be in the predetermined range described above, is preferably 3 parts by mass or less, more preferably 1.8 parts by mass or less, even more preferably 1 part by mass or less, and even more preferably 0.6 parts by mass or less from the viewpoint of enhancing cooling properties and suppressing semisolidification, and is preferably 0.005 to 3 parts by mass, more preferably 0.01 to 1.8 parts by mass, even more preferably 0.08 to 1 parts by mass, even more preferably 0.1 to
- the content of the alkali metal compound (A′) in the coolant composition of the present invention in combination with the surfactant (A) used is, with respect to the base described above (with respect to 100 g), preferably 0.5 mmol or more, more preferably 1.0 mmol or more, even more preferably 1.5 mmol or more, even more preferably 3 mmol or more, and even more preferably 5 mmol or more from the viewpoint of causing the kinematic viscosity of the coolant composition at a low temperature and a high temperature to be in the predetermined range described above, is preferably 90 mmol or less, more preferably 70 mmol or less, even more preferably 45 mmol or less, even more preferably 20 mmol or less, and even more preferably 15 mmol or less from the viewpoint of enhancing cooling properties and suppressing precipitation, and is preferably 0.5 mmol or more and 90 mmol or less, more preferably 1 mmol or more and 90 mmol or less, even more preferably 1 m
- the content of the alkali metal compound is preferably in the range described above with respect to the total amount of the base and the rust inhibitor and/or the pH adjusting agent (with respect to 100 g).
- the number of moles of the alkali metal compound is calculated by including the rust inhibitor and/or the pH adjusting agent as the alkali metal compound.
- the content of the alkali metal compound (A′) is, with respect to the base described above (with respect to 100 g), preferably 1.0 mmol or more and 90 mmol or less, and more preferably 1.0 mmol or more and 45 mmol or less.
- the content of the alkali metal compound is the total number of moles thereof.
- the number of moles of the alkali metal compound is calculated by including the rust inhibitor and/or the pH adjusting agent as the alkali metal compound.
- the content of the alkali metal compound (A′) in the coolant composition of the present invention in 100 parts by mass of the coolant composition of the present invention in combination with the surfactant (A) used is preferably 0.01 parts by mass or more, more preferably 0.02 parts by mass or more, even more preferably 0.03 parts by mass or more, even more preferably 0.05 parts by mass or more, even more preferably 0.1 parts by mass or more, even more preferably 0.25 parts by mass or more, even more preferably 0.5 parts by mass or more, and even more preferably 1 part by mass or more from the viewpoint of causing the kinematic viscosity of the coolant composition at a low temperature and a high temperature to be in the predetermined range described above, and is preferably 30 parts by mass or less, more preferably 21 parts by mass or less, even more preferably 20 parts by mass or less, even more preferably 10 parts by mass or less, even more preferably 7 parts by mass or less, and even more preferably 5 parts by mass or less from the viewpoint of enhancing cooling properties and
- the content of the alkali metal compound is preferably 0.01 to 30 parts by mass, more preferably 0.01- to 20 parts by mass, even more preferably 0.02 to 10 parts by mass, even more preferably 0.03 to 10 parts by mass, even more preferably 0.05 to 7 parts by mass, even more preferably 0.1 to 7 parts by mass, even more preferably 0.5 to 7 parts by mass, even more preferably 1 to 7 parts by mass, and even more preferably 1 to 5 parts by mass.
- the content of the alkali metal compound is calculated by including the rust inhibitor and/or the pH adjusting agent as the alkali metal compound.
- the molar ratio (alkali metal ions/surfactant) of the alkali metal ions to the surfactant (A) is preferably 1.5 or more, preferably 2.5 or more, even more preferably 3 or more, even more preferably 5 or more, even more preferably 10 or more, even more preferably 20 or more, even more preferably 30 or more, and even more preferably 40 or more from the viewpoint of causing the kinematic viscosity of the coolant composition at a low temperature and a high temperature to be in the predetermined range described above, is preferably 3000 or less, more preferably 2500 or less, even more preferably 2000 or less, even more preferably 1500 or less, even more preferably 1100 or less, even more preferably 1000 or less, even more preferably 700 or less, even more preferably 500 or less, even more preferably 300 or less, even more preferably 200 or less, and even more preferably 100 or less from the same viewpoint, and is preferably 1.5 or more and 3000 or less, more preferably 2.5
- the number of moles of the alkali metal ions is, in a case where there are a plurality of types of alkali metals, the total number of moles of the alkali metals.
- Alkali metal ions mean ions of all alkali metals in the coolant, contain not only alkali metal ions derived from the alkali metal compound but also alkali metal ions derived from the surfactant and alkali metal ions derived from other arbitrary components such as the rust inhibitor and the pH adjusting agent.
- the number of moles of the surfactant is the total number of moles of the components of the mixture.
- the coolant composition of the present invention contains the specific rubber swelling inhibitor (B).
- the rubber swelling inhibitor (B) is at least one selected from a compound expressed by the following formula (1):
- R 1 is hydrogen, a methyl group, or an ethyl group
- R 2 is hydrogen, a methyl group, or an ethyl group.
- the coolant composition of the present invention contains the surfactant (A) as the viscosity index improver
- the coolant composition can suppress swelling of rubber and discoloration of the coolant by including the rubber swelling inhibitor.
- R 1 is preferably a methyl group or an ethyl group from the viewpoint of solubility.
- R 2 is preferably a methyl group or an ethyl group from the viewpoint of solubility.
- the content of the rubber swelling inhibitor (B) in the coolant composition of the present invention in 100 parts by mass of the coolant composition of the present invention in combination with the surfactant (A) used is 0.03 parts by mass or more, preferably 0.05 parts by mass or more, more preferably 0.1 parts by mass or more, even more preferably 0.15 parts by mass or more, and even more preferably 0.2 parts by mass or more from the viewpoint of suppressing swelling of rubber, is 0.9 parts by mass or less, preferably 0.5 parts by mass or less, more preferably 0.45 parts by mass or less, even more preferably 0.4 parts by mass or less, and even more preferably 0.35 parts by mass or less from the viewpoint of suppressing discoloration of the coolant, and is 0.03 parts by mass or more and 0.9 parts by mass or less, preferably 0.05 parts by mass or more and 0.5 parts by mass or less, more preferably 0.1 parts by mass or more and 0.45 parts by mass or less, even more preferably 0.15 parts by mass or more and 0.4 parts by mass or less, and even more
- the content of the rubber swelling inhibitor (B) in the coolant composition of the present invention in combination with the surfactant (A) used is, with respect to the base described below (with respect to 100 g), preferably 0.3 mmol or more, more preferably 0.6 mmol or more, even more preferably 0.8 mmol or more, and even more preferably 1.1 mmol or more from the viewpoint of suppressing swelling of rubber, is preferably 4.0 mmol or less, more preferably 3.6 mmol or less, even more preferably 3.2 mmol or less, and even more preferably 2.8 mmol or less from the viewpoint of suppressing discoloration of the coolant, and is preferably 0.3 mmol or more and 4.0 mmol or less, more preferably 0.6 mmol or more and 3.6 mmol or less, even more preferably 0.8 mmol or more and 3.2 mmol or less, and even more preferably 1.1 mmol or more and 2.8 mmol or less from these viewpoints.
- the content of the rubber swelling inhibitor is preferably in the range described above with respect to the total amount of the base and the rust inhibitor and/or the pH adjusting agent (with respect to 100 g).
- the number of moles of the rubber swelling inhibitor is calculated by including the other additives as the rubber swelling inhibitor.
- the content of the rubber swelling inhibitor (B) is, with respect to the base described below (with respect to 100 g), preferably 0.8 mmol or more and 3.2 mmol or less, and more preferably 1.1 mmol or more and 2.8 mmol or less.
- the number of moles of the rubber swelling inhibitor is calculated by including the other additives as the rubber swelling inhibitor.
- the molar ratio (rubber swelling inhibitor/surfactant) of the rubber swelling inhibitor (B) to the surfactant (A) is preferably 0.36 or more, more preferably 0.72 or more, even more preferably 0.96 or more, and even more preferably 1.3 or more from the viewpoint of suppressing swelling of rubber, is preferably 4.8 or less, more preferably 4.3 or less, even more preferably 3.8 or less, even more preferably 3.3 or less from the viewpoint of suppressing discoloration of the coolant, and is preferably 0.36 to 4.8, more preferably 0.72 to 4.3, even more preferably from 0.96 to 3.8, and even more preferably from 1.3 to 3.3 from these viewpoints.
- the content of the rubber swelling inhibitor is calculated by including the other additives as the rubber swelling inhibitor.
- the content of the rubber swelling inhibitor is, in a case where there are a plurality of types of compounds expressed by the formula (1) and/or compounds expressed by the formula (2), the total content of the compounds expressed by the formula (1) and/or the compounds expressed by the formula (2).
- the number of moles of the rubber swelling inhibitor is, in a case where there are a plurality of types of compounds expressed by the formula (1) and/or compounds expressed by the formula (2), the total number of moles of the compounds expressed by the formula (1) and/or the compounds expressed by the formula (2).
- the base (C) used in the coolant composition of the present invention examples include water and an organic solvent, which can be used singly as water or an organic solvent, or as a mixture of water and an organic solvent. It is preferable to use a mixture of water and an organic solvent in consideration of antifreeze properties.
- the base (C) is preferably contained as a primary component.
- the “primary component” is a component that serves as the base of the coolant composition and indicates the most abundant component. If necessary, an additive or the like may be mixed in the base (C) for use in a range in which the effects of the present invention are not impaired.
- the corresponding components contained in the coolant composition of the present invention are defined as other additives, which will be described later.
- the organic solvent can be typically used in the coolant composition and is not particularly limited as long as the effects of the present invention can be obtained.
- An aqueous organic solvent is preferable, and examples thereof include at least one alcohol selected from the group consisting of a monohydric alcohol, a dihydric alcohol, a trihydric alcohol, and a glycol monoalkyl ether.
- Examples of the monohydric alcohol include one or a mixture of two or more selected from methanol, ethanol, propanol, butanol, pentanol, hexanol, heptanol, and octanol.
- dihydric alcohol examples include one or a mixture of two or more selected from ethylene glycol, diethylene glycol, triethylene glycol, propylene glycol, 1,3-propanediol, 1,4-butanediol, 1,3-butanediol, 1,5-pentanediol, and hexylene glycol.
- trihydric alcohol examples include one or a mixture of two or more selected from glycerin, trimethylolethane, trimethylolpropane, 5-methyl-1,2,4-heptanetriol, and 1,2,6-hexanetriol.
- glycol monoalkyl ether examples include one or a mixture of two or more selected from ethylene glycol monomethyl ether, diethylene glycol monomethyl ether, triethylene glycol monomethyl ether, tetraethylene glycol monomethyl ether, ethylene glycol monoethyl ether, diethylene glycol monoethyl ether, triethylene glycol monoethyl ether, tetraethylene glycol monoethyl ether, ethylene glycol monobutyl ether, diethylene glycol monobutyl ether, triethylene glycol monobutyl ether, and tetraethylene glycol monobutyl ether.
- ethylene glycol, propylene glycol, and 1,3-propanediol are preferable from the viewpoint of handleability, costs, and ease of acquisition.
- the base (C) preferably contains one or more selected from the group consisting of ethylene glycol, propylene glycol, 1,3-propanediol, and water, and more preferably contains ethylene glycol and water.
- the base (C) is preferably composed of one or more selected from the group consisting of ethylene glycol, propylene glycol, 1,3-propanediol, and water, and is more preferably composed of ethylene glycol and water. Deionized water is preferable as the water used in the base.
- the content of the base (C) is preferably 50 parts by mass or more, more preferably 75 parts by mass or more, even more preferably 80 parts by mass or more, and even more preferably 90 parts by mass or more from the viewpoint of functioning as a coolant, is preferably 99.92 parts by mass or less, more preferably 99.9 parts by mass or less, even more preferably 99.8 parts by mass or less, and even more preferably 99.7 parts by mass or less from the viewpoint of mixing the components of the coolant composition of the present invention, and is preferably 50 to 99.92 parts by mass, more preferably 80 to 99.9 parts by mass, even more preferably 90 to 99.9 parts by mass, even more preferably 90 to 99.8 parts by mass, and even more preferably 90 to 99.7 parts by mass from these viewpoints.
- the mixing ratio between water and alcohols can be arbitrarily adjusted in consideration of antifreeze properties and inflammability.
- the mass ratio between water and alcohols in the base is preferably 20:80 to 90:10 (water:alcohols), and more preferably 40:60 to 75:25 from the viewpoint of avoiding generation of a flash point.
- the kinematic viscosity at 25° C. of the coolant composition of the present invention is 8.5 mm 2 /s or more from the viewpoint of suppressing cooling loss at a low temperature, and is preferably 3000 mm 2 /s or less from the viewpoint of avoiding a load on a water pump and suppressing poor fuel efficiency of an internal combustion engine. From these viewpoints, the kinematic viscosity at 25° C. thereof is preferably 8.5 to 3000 mm 2 /s, more preferably 9 to 2000 mm 2 /s, and even more preferably 50 to 1000 mm 2 /s.
- the kinematic viscosity at 100° C. of the coolant composition of the present invention is 2.0 mm 2 /s or less, preferably 0.3 to 2.0 mm 2 /s, and more preferably 0.4 to 1.8 mm 2 /s.
- the cooling capacity of the coolant composition can be evaluated, for example, by measuring the thermal transmittance of a radiator.
- the kinematic viscosity at 100° C. of the coolant of 100% water is 0.3 mm 2 /s.
- the coolant of the present invention it is possible to set the kinematic viscosity to be in the predetermined range described above by including the components described above.
- this can be achieved by a method of increasing the content of the surfactant (A), a method of adjusting the content of the alkali metal compound (A′) in a case of using the alkali metal compound (A′), a method of increasing the content of alcohols in a case where the base (C) contains the alcohols, and the like.
- the coolant composition of the present invention may include at least one rust inhibitor in a range in which the effects of the present invention are not impaired.
- the rust inhibitor include any one or a mixture of two or more of phosphoric acid and/or a salt thereof, an aliphatic carboxylic acid and/or a salt thereof, an aromatic carboxylic acid and/or a salt thereof, a triazole, a thiazole, a silicate, a nitrate, a nitrite, a borate, a molybdate, and an amine salt.
- the coolant composition of the present invention may include at least one pH adjusting agent in a range in which the effects of the present invention are not impaired.
- the pH adjusting agent include any one or a mixture of two or more of sodium hydroxide, potassium hydroxide, and lithium hydroxide.
- the pH at 25° C. of the coolant composition of the present invention is preferably 6 or more and more preferably 7 or more, and is preferably 10 or less and more preferably 9 or less.
- a coloring agent, a dye, a dispersing agent, a bittering agent, or the like may be appropriately added in ranges in which the effects of the present invention are not impaired.
- the total amount of the above-mentioned other additives mixed therein is typically 10 parts by mass or less and preferably 5 parts by mass or less with respect to 100 parts by mass of the composition.
- a production method of the coolant composition is not particularly limited as long as the effects of the present invention can be obtained, and a typical production method of a coolant composition may be used.
- the coolant composition can be produced through uniform stirring at a low temperature.
- the coolant composition of the present invention is more preferably obtained by, after mixing, heating the mixture to preferably 60° C. or higher, more preferably 80° C. or higher and preferably 100° C. or lower, stirring the resultant if necessary, dissolving the resultant, and thereafter cooling the resultant to room temperature (20° C.).
- the present invention also relates to an automotive engine concentrated coolant composition (hereinafter, also referred to as concentrated coolant composition of the present invention).
- the concentrated coolant composition of the present invention is a composition containing the surfactant (A) as the viscosity index improver of the coolant composition of the present invention, the rubber swelling inhibitor (B), and a solvent (C′) if necessary.
- the concentrated coolant composition of the present invention can be used for obtaining the coolant composition of the present invention by being diluted, for example, 2 to 10 times by mass with the base (C).
- the solvent (C′) is a liquid that can be used in a typical coolant composition such as water and glycols, and as specific examples thereof, the above description regarding the base (C) is cited.
- the solvent (C′) may be the same as or different from the base (C).
- the concentrated coolant composition of the present invention can suppress swelling of rubber after being diluted even in a case where the surfactant (A) as the viscosity index improver, the rubber swelling inhibitor (B), and the alkali metal compound (A′) if necessary are concentrated beforehand. Therefore, the concentrated coolant composition can be used as the coolant composition by being diluted with the base (C) immediately before being supplied to the engine.
- other additives can be mixed in the concentrated coolant composition of the present invention in a range in which the effects of the present invention regarding the obtained coolant composition are not impaired. As the additives, the above description regarding the coolant composition of the present invention is cited. Furthermore, the additives may also be mixed in the solvent (C′) for use.
- An embodiment of the concentrated coolant composition of the present invention may include, with respect to 100 parts by mass of the concentrated coolant composition, the following components: (A) the surfactant as the viscosity index improver: 0.1 to 99 parts by mass; (B) the rubber swelling inhibitor: 0.1 to 5 parts by mass; and (C′) the solvent: 0 to 99.8 parts by mass.
- the concentrated coolant composition of the present invention may contain the alkali metal compound (A′).
- the content of the alkali metal compound (A′) in the concentrated coolant composition of the present invention is, with respect to 100 parts by mass of the concentrated coolant composition, preferably 1 to 30 parts by mass, and more preferably 5 to 15 parts by mass.
- the coolant composition of the present invention can be generally used as a coolant and is preferably used as a coolant for an internal combustion engine. Accordingly, the present invention also relates to a method of operating an internal combustion engine in which the coolant composition of the present invention is used as a coolant (hereinafter, also referred to as a method of operating an internal combustion engine of the present invention). According to the method of operating an internal combustion engine of the present invention, it is possible to greatly improve the fuel efficiency effect of the internal combustion engine.
- the coolant composition of the present invention can also be used as a coolant for a battery stack, a fuel cell stack, or the like.
- a rubber swelling inhibitor described in Tables 2-1 and 2-2 below a polyoxyethylene alkyl ether sulfuric acid ester salt (R c in formula (4) is a linear alkyl group having 22 carbon atoms, R d is ethylene group, q is 4, and M is sodium) as a surfactant (A) (viscosity index improver), and water were mixed in the LLC at mixing amounts (parts by mass) described in Tables 2-1 and 2-2 so that the total amount thereof reached 100 parts by mass, thereby producing coolant compositions of Examples 1 to 6 and coolant compositions of Comparative Examples 1 to 11.
- the polyoxyethylene alkyl ether sulfuric acid ester salt was synthesized as follows.
- an alcohol ethoxylate (the average number of moles of ethylene oxide added was 4.0) of a higher alcohol primarily containing 22 carbon atoms (trade name: KALCOL 220-80 manufactured by Kao corporation) was caused to flow down in a thin film form at a supply rate of 5.0 L/h, and sulfur trioxide gas diluted with dry air (concentration of sulfur trioxide gas: 1.1 vol %) was added under conditions of a reactor cooling temperature of 40° C. and a supply rate of 130 L/min (molar ratio of sulfur trioxide/ethoxylate:1.00) to carry out a sulfation reaction.
- the obtained polyoxyethylene alkyl ether sulfate was neutralized by a 2.5% sodium hydroxide aqueous solution (molar ratio of sodium hydroxide/polyoxyethylene alkyl ether sulfuric acid ester: 1.10) so as to cause the concentration of polyoxyethylene ether sodium sulfate to be 23% or more and 27% or less such that polyoxyethylene alkyl ether sodium sulfate having 22 carbon atoms (the average number of moles of ethylene oxide added was 4.0) was synthesized.
- the obtained coolant compositions were subjected to the following evaluation tests.
- the kinematic viscosity at 25° C. was measured according to JIS K 2283. A case where the kinematic viscosity at 25° C. of the coolant composition was 8.5 mm 2 /s or higher was evaluated as good.
- the temperature of the coolant was set to 120° C., a test piece of H-NBR rubber was immersed under an oxygen pressure of 0.1 MPa for 1000 hours, and the rate of change in the volume of the test piece after immersion was measured. A rate of change in the volume of 30% or less was evaluated as good.
- Example 2 Compo- LLC 53 53 53 53 53 53 53 53 53 53 53 sition Water 46.45 46 46.45 46 46.45 46 47 46.5 Viscosity Polyoxyethylene 0.5 0.5 0.5 0.5 0.5 0.5 0.5 — 0.5 index alkyl ether sulfuric improver acid ester salt Rubber Methyl 3,5- 0.05 0.5 0.025 0.25 — swelling dihydroxybenzoate inhibitor p-methoxyphenol 0.05 0.5 0.025 0.25 — t-butylhydroquinone Methyl gallate — 4-t-butylpyrocatechol 3,3′- — dithiodipropionic acid Evalu- A rate of change in the 23 6 27 6 23 7 6 63 ation volume of rubber (H-NBR) of 30% or less is good Discoloration test No No No No No No No No No significant significant significant significant significant significant significant significant significant significant significant significant significant significant significant discolor- discolor- discolor- discolor- discolor- discolor- discolor- discolor- discolor- discolor
- the coolant composition of the present invention is suitably used for cooling an internal combustion engine, particularly an automotive engine, an inverter, a battery, and the like.
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Abstract
Description
- The present invention relates to an automotive engine coolant composition, an automotive engine concentrated coolant composition, and a method of operating an internal combustion engine.
- Various types of coolant for cooling automotive engines and the like are known, and among the coolants, water has been widely used as engine coolant because of its highest cooling performance. However, so-called pure water, which does not contain an electrolyte and the like, freezes at 0° C. or lower, and increases in volume, possibly leading to damage to the engine and radiator. Therefore, a coolant composition, which does not use only pure water, and is formed by using a glycol such as ethylene glycol as the base for the purpose of antifreeze properties, diluting this with water so as to obtain a required freezing temperature, and mixing various additives for protecting metals, rubbers, resins, and the like used in the engine or radiator from deterioration as necessary therein has been used.
- However, in a case where glycols such as ethylene glycol are used, there is a possibility that the viscosity of the coolant composition may significantly increase particularly at a low temperature. Therefore, in order to adjust the viscosity of the coolant, a viscosity index improver is mixed therein (Japanese Patent No. 5904278), and a technique for prompting quick warm-up of the engine and improving fuel efficiency by mixing a surfactant as a viscosity index improver in a coolant and thus appropriately increasing viscosity has been carried out. On the other hand, since the surfactant has the drawback of swelling the rubber used in automotive parts, an antioxidant has been blended in order to suppress the volume change of the rubber under the immersion environment in the coolant.
- For example, in Japanese Patent Application Publication No. 2009-242663 (JP 2009-242663 A), it is described that a sulfur-containing alcohol or a phenol-based antioxidant is mixed in a rubber swelling antifreeze/coolant composition containing an aliphatic monobasic acid. In WO2004/050785, it is described that hydroxybenzoic acid, isocitric acid, acetylsalicylic acid, and the like are mixed as additives for improving the thermal stability of glycol components. In WO2005/054398, it is described that by mixing gallic acid, derivatives of gallic acid, or catechols in a coolant composition containing a glycol as a primary component and an aliphatic carboxylic acid or an aromatic carboxylic acid, blackening of aluminum or aluminum alloys is prevented. In GB961409, it is described that a hydroxy compound (catechol) as an antioxidant is mixed in a coolant. In Japanese Patent Publication No. 2-51988, it is described that resorcinol, fluoroglycine, and the like are mixed in a coolant for calcium chloride brine.
- However, the coolant mixed with the antioxidant as described above has a possibility that there may be insufficient effect in suppressing swelling of rubber or the coolant may be significantly discolored.
- The present invention provides an automotive engine coolant composition which has a specific kinematic viscosity and is capable of suppressing swelling of contacting rubber and discoloration of a coolant. The present invention also provides an automotive engine concentrated coolant composition for obtaining such an automotive engine coolant composition.
- As a result of intensive studies to solve the above problems, the inventors completed the present invention by combining a coolant composition containing a surfactant and a base with a specific rubber swelling inhibitor in a specific amount.
- That is, the present invention includes the following inventions.
- [1] An automotive engine coolant composition including: a surfactant as a viscosity index improver; a rubber swelling inhibitor; and a base, in which
- the rubber swelling inhibitor is at least one selected from a compound expressed by a following formula (1):
- [In the formula, R1 is hydrogen, a methyl group, or an ethyl group], and a compound expressed by a following formula (2):
- [in the formula, R2 is hydrogen, a methyl group, or an ethyl group], the base includes at least one alcohol selected from the group consisting of a monohydric alcohol, a dihydric alcohol, a trihydric alcohol, and a glycol monoalkyl ether and/or water and has a kinematic viscosity of 8.5 mm2/s or more at 25° C., and a content of the rubber swelling inhibitor is 0.03 parts by mass or more and 0.9 parts by mass or less with respect to 100 parts by mass of the coolant composition.
- [2] The coolant composition according to [1], in which the coolant composition may have a kinematic viscosity of 2.0 mm2/s or less at 100° C.
- [3] The coolant composition according to [1] or [2], in which the content of the rubber swelling inhibitor may be 0.05 parts by mass or more and 0.5 parts by mass or less with respect to 100 parts by mass of the coolant composition.
- [4] The coolant composition according to any one of [1] to [3], a content of the surfactant may be 0.005 parts by mass or more and 3 parts by mass or less with respect to 100 parts by mass of the coolant composition.
- [5] The coolant composition according to any one of [1] to [4], which may further include a rust inhibitor.
- [6] The coolant composition according to any one of [1] to [5], in which the base may contain an organic solvent.
- [7] An automotive engine concentrated coolant composition for obtaining the coolant composition according to any one of [1] to [6], which is diluted 2 to 10 times by mass with a base so as to be used.
- [8] The concentrated coolant composition according to [7], in which, with respect to 100 parts by mass of the concentrated coolant composition, a surfactant as a viscosity index improver: 0.1 to 99 parts by mass; a rubber swelling inhibitor: 0.1 to 5 parts by mass; and a solvent: 0 to 99.8 parts by mass may be contained.
- [9] A method of operating an internal combustion engine, which uses the coolant composition according to any one of [1] to [6] as a coolant.
- The automotive engine coolant composition of the present invention has a specific kinematic viscosity and thus can improve the fuel efficiency effect of an internal combustion engine. In addition, the automotive engine coolant composition of the present invention can suppress swelling of rubber used in automotive parts while suppressing discoloration of the coolant. In addition, the automotive engine coolant composition can be obtained by diluting the automotive engine concentrated coolant composition of the present invention.
- Features, advantages, and technical and industrial significance of exemplary embodiments of the invention will be described below with reference to the accompanying drawings, in which like numerals denote like elements, and wherein:
-
FIG. 1A is a diagram showing a putative mechanism for swelling of rubber; -
FIG. 1B is a diagram showing a putative mechanism for swelling of rubber; -
FIG. 1C is a diagram showing a putative mechanism for swelling of rubber; -
FIG. 1D is a diagram showing a putative mechanism for swelling of rubber; and -
FIG. 1E is a diagram showing a putative mechanism for swelling of rubber. - An automotive engine coolant composition of the present invention (hereinafter, also referred to as a coolant composition of the present invention) includes a surfactant (A) as a viscosity index improver, a specific rubber swelling inhibitor (B), and a base (C). The inventors found that by combining a coolant composition containing a surfactant as a viscosity index improver and a base with a specific rubber swelling inhibitor, a specific kinematic viscosity is imparted due to an appropriate thickening effect exhibited by the surfactant, and it becomes possible to suppress swelling of contacting rubber and discoloration of the coolant. A coolant mixed with an antioxidant of the related art, particularly a phenolic antioxidant is not effective enough to suppress swelling of rubber and causes significant discoloration. However, the coolant composition of the present invention mixed with the specific rubber swelling inhibitor (B) is excellent both in suppression of swelling of rubber and suppression of discoloration. Although the details of mechanisms for causing the specific kinematic viscosity to be exhibited due to an appropriate thickening effect of the viscosity index improver according to the present invention are not clear, the following is conceivable. That is, it is conceivable that as the viscosity index improver is present in a coolant, a complex with the base is formed, a certain type of structure is formed in the coolant, and the structure can be changed by a change in temperature, so that the viscosity characteristics of the coolant can be adjusted. However, it should not be construed as being limited to the mechanisms.
- Although not restrained by theory, it is conceivable that in the coolant composition of the present invention, the rubber swelling inhibitor (B) suppresses oxidation deterioration due to oxygen brought into rubber by the surfactant such that it becomes possible to suppress swelling of rubber. A putative mechanism for swelling of rubber in a coolant mixed with a surfactant is illustrated in
FIGS. 1A to 1E . First, a hydrophobic group of the surfactant as a viscosity index improver penetrates into the rubber contacting the coolant (FIGS. 1A and 1B ), and a hydrophilic group of the surfactant brings the coolant in which oxygen is dissolved into the rubber such that the rubber is swelled (FIG. 1C ). Oxygen brought into the rubber oxidizes and deteriorates the rubber and the cross-link density of the rubber decreases due to breaking of the molecular chain and introduction of oxygen atoms into the molecule (FIG. 1D ). The surfactant and the coolant in which oxygen is dissolved are further brought into and penetrate into the dense rubber surface layer, and the rubber is swelled (FIG. 1E ). The penetrated oxygen further oxidized and deteriorated the rubber, and the surfactant further brings the coolant in which oxygen is dissolved into the rubber, resulting in an increase in the swelling of the rubber (FIG. 1E ). - In this specification, the term “rubber” refers to those that are in contact with an automotive engine coolant, such as an automotive engine, an inverter, a battery, and hoses. Specific examples thereof include ethylene propylene diene rubber (EPDM), hydrogenated nitrile rubber (H-NBR), nitrile rubber (NBR), fluoro rubber (FKM), and silicone rubber (VMQ). The coolant composition of the present invention has a structure such as a carbon-hydrogen bond in the polymer backbone chain of the rubber molecule, and oxygen is incorporated by the surfactant. Therefore, the coolant composition exhibits particularly desirable effects on rubber in which breaking of the molecular chain and introduction of oxygen atoms into the molecule easily occur.
- In this specification, a “low temperature” means, for example, 25° C. and a “high temperature” means, for example, 100° C.
- The surfactant (A) used in the coolant composition of the present invention can be typically used as a viscosity index improver in the coolant composition and is not particularly limited as long as the effects of the present invention can be obtained. The surfactant (A) may be any of a nonionic surfactant, an anionic surfactant, a cationic surfactant, and an amphoteric surfactant. One type of the surfactant (A) may be used singly, or two or more types thereof may be used in combination.
- Specific examples of the nonionic surfactant include a compound having a polyalkylene glycol chain, an ester of a fatty acid with a polyhydric alcohol such as glycerin, sorbitol, or sucrose, a fatty acid alkanolamide, and the like. From the viewpoint of heat resistance and water solubility, a compound having a polyalkylene glycol chain is preferable, and a compound having a polyethylene glycol chain is more preferable. Examples of the compound having a polyethylene glycol chain include polyoxyethylene polyoxypropylene glycol, polyoxyethylene monoalkyl ether, polyoxyethylene dialkyl ether, polyoxyethylene polyoxypropylene alkyl ether, polyoxyethylene alkyl phenyl ether, polyethylene glycol polyhydric alcohol ether, polyethylene glycol alkyl amino ether, polyethylene glycol mono fatty acid ester, polyethylene glycol difatty acid ester, polyoxyethylene sorbitan fatty acid ester, polyoxyethylene sorbitol fatty acid ester, polyoxyethylene glycerin fatty acid ester, polyoxyethylene castor oil, polyoxyethylene hydrogenated castor oil, and polyoxyethylene fatty acid amide. Among these, polyoxyethylene monoalkyl ether, fatty acid alkanol amide, polyethylene glycol difatty acid ester, and polyoxyethylene fatty acid amide, which greatly increase in kinematic viscosity at 25° C. and slightly increase in kinematic viscosity at 100° C. in a low mixing amount, are preferable, and polyoxyethylene monoalkyl ether is more preferable.
- The polyoxyalkylene alkyl ether is preferably a compound represented by the following formula (3):
-
RaO—(RbO)p—H (3) - [in the formula, Ra is a linear or branched alkyl or alkenyl group having 12 or more and 24 or less carbon atoms, Rb is an ethylene group or a propylene group, p represents an average number of moles of RbO added, and is a number from 0.5 or more and 20 or less.]
- Regarding Ra mentioned above, the alkyl group or alkenyl group may be linear or branched, and is preferably linear from the viewpoint of thickening effect. The number of carbon atoms of the alkyl group or alkenyl group is preferably 12 or more and 24 or less, more preferably 16 or more and 22 or less, and even more preferably 20 or more and 22 or less.
- Specific examples thereof include: an alkyl group such as a lauryl group, a myristyl group, a cetyl group, a margaryl group, an isostearyl group, a 2-heptylundecyl group, a stearyl group, an arachidyl group, a behenyl group, and a lignoceryl group; and an alkenyl group such as an oleyl group. A cetyl group, a stearyl group, and a behenyl group are preferable, and a stearyl group and a behenyl group are more preferable.
- Rb mentioned above is preferably an ethylene group or a propylene group, and is more preferably an ethylene group from the viewpoint of thickening effect.
- p mentioned above represents the average number of moles of RbO added, and from the viewpoint of thickening effect, is preferably a number from 0.5 or more and 20 or less, more preferably a number from 1 or more and 15 or less, even more preferably a number from 2 or more and 11 or less, and even more preferably a number from 3 or more and 8 or less.
- Examples of the anionic surfactant include an alkyl sulfuric acid ester salt, a polyoxyethylene alkyl ether sulfuric acid ester salt, an alkylbenzene sulfonic acid salt, a fatty acid salt, an alkyl phosphoric acid ester salt, and a polyoxyethylene alkyl ether phosphoric acid ester salt. A polyoxyethylene alkyl ether sulfuric acid ester salt, which greatly increases in kinematic viscosity at 25° C. and slightly increases in kinematic viscosity at 100° C. in a low mixing amount, is preferable.
- The polyoxyethylene alkyl ether sulfuric acid ester salt is preferably a compound represented by the following formula (4):
-
RcO—(RdO)q—SO3M (4) - [in the formula, Rc is a linear or branched alkyl or alkenyl group having 16 or more and 24 or less carbon atoms, Rd is an ethylene group or a propylene group, q represents an average number of moles of RdO added, and is a number from 0.5 or more and 10 or less, and M is a cation or a hydrogen atom.]
- Regarding Rc mentioned above, the alkyl group may be linear or branched, and is preferably linear from the viewpoint of thickening effect. The number of carbon atoms of the alkyl group and the alkenyl group is preferably 16 or more and 24 or less, more preferably 18 or more and 22 or less, and even more preferably 20 or more and 22 or less.
- Specific examples thereof include: an alkyl group such as a cetyl group, a margaryl group, an isostearyl group, a 2-heptylundecyl group, a stearyl group, an arachidyl group, a behenyl group, a lignoceryl group; and an alkenyl group such as an oleyl group. A cetyl group, a stearyl group, an arachidyl group, and a behenyl group are preferable, and a behenyl group is more preferable.
- Rd mentioned above is preferably an ethylene group or a propylene group, and is more preferably an ethylene group from the viewpoint of thickening effect.
- q mentioned above represents the average number of moles of RdO added, and from the viewpoint of having a specific kinematic viscosity at a low temperature and a high temperature, is preferably a number from 0.5 or more and 10 or less, and more preferably a number from 1 or more and 8 or less, even more preferably a number from 2 or more and 7 or less, and even more preferably a number from 3 or more and 6 or less.
- M mentioned above is a cation or a hydrogen atom, and is preferably a cation. Specific examples of the cation include an alkali metal ion and an ammonium ion, and examples of the alkali metal include lithium, sodium, and potassium. Sodium or potassium is preferable.
- Examples of the cationic surfactant include an alkylamine salt and a quaternary ammonium salt.
- Examples of the amphoteric surfactant include an alkylbetaine and an alkylamine oxide.
- The surfactant (A) used in the coolant composition of the present invention can be typically used as a viscosity index improver in the coolant composition and is not particularly limited as long as the effects of the present invention can be obtained. From the viewpoint of thickening effect, a nonionic surfactant or an anionic surfactant is preferable, and an anionic surfactant is more preferable.
- The coolant composition of the present invention may contain an alkali metal compound (A′). In a case where the surfactant (A) used is an anionic surfactant, particularly an anionic surfactant represented by the formula (4), the alkali metal compound (A′) is preferably contained.
- The alkali metal compound (A′) is at least one type selected from the group consisting of an alkali metal salt and an alkali metal hydroxide, and the alkali metal salt excludes the surfactant (A). Examples of the alkali metal include sodium, potassium, and lithium. Examples of the alkali metal salt include an alkali metal salt of an inorganic acid or an organic acid, and an alkali metal salt of a triazole or a thiazole. Examples of the alkali metal salt of an inorganic acid include an alkali metal salt of nitrous acid such as sodium nitrite and potassium nitrite; an alkali metal salt of nitric acid such as sodium nitrate and potassium nitrate; an alkali metal salt of molybdic acid such as sodium molybdate and potassium molybdate; an alkali metal salt of hypochlorous acid such as sodium hypochlorite and potassium hypochlorite; an alkali metal salt of sulfuric acid such as sodium sulfate and potassium sulfate; an alkali metal salts of carbonic acid such as sodium carbonate and potassium carbonate; an alkali metal salt of hydrochloric acid such as sodium chloride and potassium chloride; an alkali metal salt of phosphoric acid such as sodium phosphate and potassium phosphate; an alkali metal salt of silicic acid such as sodium silicate and potassium silicate; and an alkali metal salt of boric acid such as sodium borate and potassium borate. Examples of the alkali metal salt of an organic acid include an alkali metal salt of an aromatic carboxylic acid such as benzoic acid, p-toluic acid, and p-tertbutylbenzoic acid; and an alkali metal salt of an aliphatic polyvalent carboxylic acid such as azelaic acid, sebacic acid, undecanedioic acid, dodecanedioic acid, and citric acid. Examples of the alkali metal salt of a triazole or a thiazole include an alkali metal salt of benzotriazole. Among the above-mentioned alkali metal salts, an alkali metal salt of an aliphatic polyvalent carboxylic acid is preferable from the viewpoint of causing the kinematic viscosity of the coolant composition at a low temperature and a high temperature to be in the predetermined range described above, and dipotassium sebacate is more preferable. In a case where an alkali metal salt is used as a rust inhibitor and/or a pH adjusting agent, it is presumed that this is used as the alkali metal salt. In that case, an alkali metal compound does not necessarily need to be separately added.
- The alkali metal hydroxide is not particularly limited, and specific examples thereof include lithium hydroxide, sodium hydroxide, and potassium hydroxide. Among the above-mentioned alkali metal hydroxides, potassium hydroxide is preferable from the viewpoint of causing the kinematic viscosity of the coolant composition at a low temperature and a high temperature to be in the predetermined range described above.
- The content of the surfactant (A) in the coolant composition of the present invention is, with respect to the base described above (with respect to 100 g), preferably 0.01 mmol or more, more preferably 0.05 mmol or more, even more preferably 0.1 mmol or more, even more preferably 0.15 mmol or more, even more preferably 0.2 mmol or more, even more preferably 0.25 mmol or more, even more preferably 0.3 mmol or more, and even more preferably 0.4 mmol or more from the viewpoint of causing the kinematic viscosity of the coolant composition at a low temperature and a high temperature to be in the predetermined range described above, is preferably 3 mmol or less, more preferably 2 mmol or less, even more preferably 1 mmol or less, and even more preferably 0.8 mmol or less from the viewpoint of enhancing cooling properties and suppressing semisolidification, and is preferably 0.01 mmol or more and 3 mmol or less, more preferably 0.05 mmol or more and 3 mmol or less, even more preferably 0.1 mmol or more and 2 mmol or less, even more preferably 0.2 mmol or more and 1 mmol or less, even more preferably 0.25 mmol or more and 0.8 mmol or less, even more preferably 0.3 mmol or more and 0.8 mmol or less, and even more preferably 0.4 mmol or more and 0.8 mmol or less from these viewpoints. In the case of using the rust inhibitor and/or the pH adjusting agent, the content of the surfactant (A) is preferably in the range described above with respect to the total amount of the base and the rust inhibitor and/or the pH adjusting agent (with respect to 100 g).
- In addition, in another embodiment of the coolant composition of the present invention, the content of the surfactant (A) in 100 parts by mass of the coolant composition of the present invention is preferably 0.005 parts by mass or more, more preferably 0.01 parts by mass or more, even more preferably 0.05 parts by mass or more, even more preferably 0.08 parts by mass or more, even more preferably 0.1 parts by mass or more, and even more preferably 0.2 parts by mass or more from the viewpoint of causing the kinematic viscosity of the coolant composition at a low temperature and a high temperature to be in the predetermined range described above, is preferably 3 parts by mass or less, more preferably 1.8 parts by mass or less, even more preferably 1 part by mass or less, and even more preferably 0.6 parts by mass or less from the viewpoint of enhancing cooling properties and suppressing semisolidification, and is preferably 0.005 to 3 parts by mass, more preferably 0.01 to 1.8 parts by mass, even more preferably 0.08 to 1 parts by mass, even more preferably 0.1 to 0.6 parts by mass, and even more preferably 0.2 to 0.6 parts by mass from these viewpoints.
- The content of the alkali metal compound (A′) in the coolant composition of the present invention in combination with the surfactant (A) used is, with respect to the base described above (with respect to 100 g), preferably 0.5 mmol or more, more preferably 1.0 mmol or more, even more preferably 1.5 mmol or more, even more preferably 3 mmol or more, and even more preferably 5 mmol or more from the viewpoint of causing the kinematic viscosity of the coolant composition at a low temperature and a high temperature to be in the predetermined range described above, is preferably 90 mmol or less, more preferably 70 mmol or less, even more preferably 45 mmol or less, even more preferably 20 mmol or less, and even more preferably 15 mmol or less from the viewpoint of enhancing cooling properties and suppressing precipitation, and is preferably 0.5 mmol or more and 90 mmol or less, more preferably 1 mmol or more and 90 mmol or less, even more preferably 1 mmol or more and 70 mmol or less, even more preferably 1 mmol or more and 45 mmol or less, even more preferably 1.5 mmol or more and 20 mmol or less, even more preferably 3 mmol or more and 20 mmol or less, and even more preferably 5 mmol or more and 15 mmol or less from these viewpoints. In the case of using the rust inhibitor and/or the pH adjusting agent, the content of the alkali metal compound is preferably in the range described above with respect to the total amount of the base and the rust inhibitor and/or the pH adjusting agent (with respect to 100 g). In addition, in the case of using the rust inhibitor and/or the pH adjusting agent, the number of moles of the alkali metal compound is calculated by including the rust inhibitor and/or the pH adjusting agent as the alkali metal compound.
- In a case of being used together with C22H45O—(CH2CH2O)4—SO3Na or C22H45O—(CH2CH2O)4—SO3K as the surfactant (A), the content of the alkali metal compound (A′) is, with respect to the base described above (with respect to 100 g), preferably 1.0 mmol or more and 90 mmol or less, and more preferably 1.0 mmol or more and 45 mmol or less. In a case where both an alkali metal salt and an alkali metal hydroxide are used, the content of the alkali metal compound is the total number of moles thereof. In the case of using an alkali metal compound as the rust inhibitor and/or the pH adjusting agent, the number of moles of the alkali metal compound is calculated by including the rust inhibitor and/or the pH adjusting agent as the alkali metal compound.
- The content of the alkali metal compound (A′) in the coolant composition of the present invention in 100 parts by mass of the coolant composition of the present invention in combination with the surfactant (A) used is preferably 0.01 parts by mass or more, more preferably 0.02 parts by mass or more, even more preferably 0.03 parts by mass or more, even more preferably 0.05 parts by mass or more, even more preferably 0.1 parts by mass or more, even more preferably 0.25 parts by mass or more, even more preferably 0.5 parts by mass or more, and even more preferably 1 part by mass or more from the viewpoint of causing the kinematic viscosity of the coolant composition at a low temperature and a high temperature to be in the predetermined range described above, and is preferably 30 parts by mass or less, more preferably 21 parts by mass or less, even more preferably 20 parts by mass or less, even more preferably 10 parts by mass or less, even more preferably 7 parts by mass or less, and even more preferably 5 parts by mass or less from the viewpoint of enhancing cooling properties and suppressing precipitation. From these viewpoints, the content of the alkali metal compound is preferably 0.01 to 30 parts by mass, more preferably 0.01- to 20 parts by mass, even more preferably 0.02 to 10 parts by mass, even more preferably 0.03 to 10 parts by mass, even more preferably 0.05 to 7 parts by mass, even more preferably 0.1 to 7 parts by mass, even more preferably 0.5 to 7 parts by mass, even more preferably 1 to 7 parts by mass, and even more preferably 1 to 5 parts by mass. In the case of using an alkali metal compound as the rust inhibitor and/or the pH adjusting agent, the content of the alkali metal compound is calculated by including the rust inhibitor and/or the pH adjusting agent as the alkali metal compound.
- In the coolant composition of the present invention, the molar ratio (alkali metal ions/surfactant) of the alkali metal ions to the surfactant (A) is preferably 1.5 or more, preferably 2.5 or more, even more preferably 3 or more, even more preferably 5 or more, even more preferably 10 or more, even more preferably 20 or more, even more preferably 30 or more, and even more preferably 40 or more from the viewpoint of causing the kinematic viscosity of the coolant composition at a low temperature and a high temperature to be in the predetermined range described above, is preferably 3000 or less, more preferably 2500 or less, even more preferably 2000 or less, even more preferably 1500 or less, even more preferably 1100 or less, even more preferably 1000 or less, even more preferably 700 or less, even more preferably 500 or less, even more preferably 300 or less, even more preferably 200 or less, and even more preferably 100 or less from the same viewpoint, and is preferably 1.5 or more and 3000 or less, more preferably 2.5 or more and 3000 or less, even more preferably 3 or more and 2500 or less, even more preferably 5 or more and 2000 or less, even more preferably 5 or more and 1500 or less, even more preferably 10 or more and 1000 or less, even more preferably 10 or more and 700 or less, even more preferably 20 or more and 500 or less, even more preferably 30 or more and 300 or less, even more preferably 30 or more and 200 or less, even more preferably 30 or more and 100 or less, and even more preferably 40 or more and 100 or less from these viewpoints.
- The number of moles of the alkali metal ions is, in a case where there are a plurality of types of alkali metals, the total number of moles of the alkali metals. Alkali metal ions mean ions of all alkali metals in the coolant, contain not only alkali metal ions derived from the alkali metal compound but also alkali metal ions derived from the surfactant and alkali metal ions derived from other arbitrary components such as the rust inhibitor and the pH adjusting agent. In addition, in a case where the surfactant is a mixture, the number of moles of the surfactant is the total number of moles of the components of the mixture.
- The coolant composition of the present invention contains the specific rubber swelling inhibitor (B). The rubber swelling inhibitor (B) is at least one selected from a compound expressed by the following formula (1):
- [In the formula, R1 is hydrogen, a methyl group, or an ethyl group], and a compound expressed by the following formula (2):
- [in the formula, R2 is hydrogen, a methyl group, or an ethyl group].
- Although the coolant composition of the present invention contains the surfactant (A) as the viscosity index improver, the coolant composition can suppress swelling of rubber and discoloration of the coolant by including the rubber swelling inhibitor.
- The action of the compound expressed by the formula (1) or (2) on rubber is not restrained by theory. However, it is conceivable that oxidation deterioration of rubber is a radical chain reaction, rubber molecules as radicals react with themselves such that the rubber molecules are reduced. In the compound expressed by the formula (1), R1 is preferably a methyl group or an ethyl group from the viewpoint of solubility. In the compound expressed by the formula (2), R2 is preferably a methyl group or an ethyl group from the viewpoint of solubility.
- The content of the rubber swelling inhibitor (B) in the coolant composition of the present invention in 100 parts by mass of the coolant composition of the present invention in combination with the surfactant (A) used is 0.03 parts by mass or more, preferably 0.05 parts by mass or more, more preferably 0.1 parts by mass or more, even more preferably 0.15 parts by mass or more, and even more preferably 0.2 parts by mass or more from the viewpoint of suppressing swelling of rubber, is 0.9 parts by mass or less, preferably 0.5 parts by mass or less, more preferably 0.45 parts by mass or less, even more preferably 0.4 parts by mass or less, and even more preferably 0.35 parts by mass or less from the viewpoint of suppressing discoloration of the coolant, and is 0.03 parts by mass or more and 0.9 parts by mass or less, preferably 0.05 parts by mass or more and 0.5 parts by mass or less, more preferably 0.1 parts by mass or more and 0.45 parts by mass or less, even more preferably 0.15 parts by mass or more and 0.4 parts by mass or less, and even more preferably 0.2 parts by mass or more and 0.35 parts by mass or less from these viewpoints. In a case of using the compound expressed by the formula (1) and/or (2) as other additives such as a rust inhibitor, which will be described later, the content of the rubber swelling inhibitor is calculated by including the other additives as the rubber swelling inhibitor.
- The content of the rubber swelling inhibitor (B) in the coolant composition of the present invention in combination with the surfactant (A) used is, with respect to the base described below (with respect to 100 g), preferably 0.3 mmol or more, more preferably 0.6 mmol or more, even more preferably 0.8 mmol or more, and even more preferably 1.1 mmol or more from the viewpoint of suppressing swelling of rubber, is preferably 4.0 mmol or less, more preferably 3.6 mmol or less, even more preferably 3.2 mmol or less, and even more preferably 2.8 mmol or less from the viewpoint of suppressing discoloration of the coolant, and is preferably 0.3 mmol or more and 4.0 mmol or less, more preferably 0.6 mmol or more and 3.6 mmol or less, even more preferably 0.8 mmol or more and 3.2 mmol or less, and even more preferably 1.1 mmol or more and 2.8 mmol or less from these viewpoints. In the case of using the rust inhibitor and/or the pH adjusting agent, the content of the rubber swelling inhibitor is preferably in the range described above with respect to the total amount of the base and the rust inhibitor and/or the pH adjusting agent (with respect to 100 g). In the case of using the compound expressed by the formula (1) and/or (2) as other additives such as the rust inhibitor, which will be described later, the number of moles of the rubber swelling inhibitor is calculated by including the other additives as the rubber swelling inhibitor.
- In a case of being used together with C22H45O—(CH2CH2O)4—SO3Na or C22H45O—(CH2CH2O)4—SO3K as the surfactant (A), the content of the rubber swelling inhibitor (B) is, with respect to the base described below (with respect to 100 g), preferably 0.8 mmol or more and 3.2 mmol or less, and more preferably 1.1 mmol or more and 2.8 mmol or less. In the case of using the compound expressed by the formula (1) and/or (2) as other additives such as the rust inhibitor, which will be described later, the number of moles of the rubber swelling inhibitor is calculated by including the other additives as the rubber swelling inhibitor.
- In the coolant composition of the present invention, the molar ratio (rubber swelling inhibitor/surfactant) of the rubber swelling inhibitor (B) to the surfactant (A) is preferably 0.36 or more, more preferably 0.72 or more, even more preferably 0.96 or more, and even more preferably 1.3 or more from the viewpoint of suppressing swelling of rubber, is preferably 4.8 or less, more preferably 4.3 or less, even more preferably 3.8 or less, even more preferably 3.3 or less from the viewpoint of suppressing discoloration of the coolant, and is preferably 0.36 to 4.8, more preferably 0.72 to 4.3, even more preferably from 0.96 to 3.8, and even more preferably from 1.3 to 3.3 from these viewpoints. In the case of using the compound expressed by the formula (1) and/or (2) as other additives such as a rust inhibitor, which will be described later, the content of the rubber swelling inhibitor is calculated by including the other additives as the rubber swelling inhibitor.
- The content of the rubber swelling inhibitor is, in a case where there are a plurality of types of compounds expressed by the formula (1) and/or compounds expressed by the formula (2), the total content of the compounds expressed by the formula (1) and/or the compounds expressed by the formula (2). In addition, the number of moles of the rubber swelling inhibitor is, in a case where there are a plurality of types of compounds expressed by the formula (1) and/or compounds expressed by the formula (2), the total number of moles of the compounds expressed by the formula (1) and/or the compounds expressed by the formula (2).
- Examples of the base (C) used in the coolant composition of the present invention include water and an organic solvent, which can be used singly as water or an organic solvent, or as a mixture of water and an organic solvent. It is preferable to use a mixture of water and an organic solvent in consideration of antifreeze properties. In the coolant composition of the present invention, the base (C) is preferably contained as a primary component. Here, the “primary component” is a component that serves as the base of the coolant composition and indicates the most abundant component. If necessary, an additive or the like may be mixed in the base (C) for use in a range in which the effects of the present invention are not impaired. In this specification, the corresponding components contained in the coolant composition of the present invention are defined as other additives, which will be described later.
- The organic solvent can be typically used in the coolant composition and is not particularly limited as long as the effects of the present invention can be obtained. An aqueous organic solvent is preferable, and examples thereof include at least one alcohol selected from the group consisting of a monohydric alcohol, a dihydric alcohol, a trihydric alcohol, and a glycol monoalkyl ether.
- Examples of the monohydric alcohol include one or a mixture of two or more selected from methanol, ethanol, propanol, butanol, pentanol, hexanol, heptanol, and octanol.
- Examples of the dihydric alcohol include one or a mixture of two or more selected from ethylene glycol, diethylene glycol, triethylene glycol, propylene glycol, 1,3-propanediol, 1,4-butanediol, 1,3-butanediol, 1,5-pentanediol, and hexylene glycol.
- Examples of the trihydric alcohol include one or a mixture of two or more selected from glycerin, trimethylolethane, trimethylolpropane, 5-methyl-1,2,4-heptanetriol, and 1,2,6-hexanetriol.
- Examples of the glycol monoalkyl ether include one or a mixture of two or more selected from ethylene glycol monomethyl ether, diethylene glycol monomethyl ether, triethylene glycol monomethyl ether, tetraethylene glycol monomethyl ether, ethylene glycol monoethyl ether, diethylene glycol monoethyl ether, triethylene glycol monoethyl ether, tetraethylene glycol monoethyl ether, ethylene glycol monobutyl ether, diethylene glycol monobutyl ether, triethylene glycol monobutyl ether, and tetraethylene glycol monobutyl ether.
- Among the above-mentioned organic solvents, ethylene glycol, propylene glycol, and 1,3-propanediol are preferable from the viewpoint of handleability, costs, and ease of acquisition.
- Therefore, the base (C) preferably contains one or more selected from the group consisting of ethylene glycol, propylene glycol, 1,3-propanediol, and water, and more preferably contains ethylene glycol and water. In addition, the base (C) is preferably composed of one or more selected from the group consisting of ethylene glycol, propylene glycol, 1,3-propanediol, and water, and is more preferably composed of ethylene glycol and water. Deionized water is preferable as the water used in the base.
- In 100 parts by mass of the coolant composition of the present invention, the content of the base (C) is preferably 50 parts by mass or more, more preferably 75 parts by mass or more, even more preferably 80 parts by mass or more, and even more preferably 90 parts by mass or more from the viewpoint of functioning as a coolant, is preferably 99.92 parts by mass or less, more preferably 99.9 parts by mass or less, even more preferably 99.8 parts by mass or less, and even more preferably 99.7 parts by mass or less from the viewpoint of mixing the components of the coolant composition of the present invention, and is preferably 50 to 99.92 parts by mass, more preferably 80 to 99.9 parts by mass, even more preferably 90 to 99.9 parts by mass, even more preferably 90 to 99.8 parts by mass, and even more preferably 90 to 99.7 parts by mass from these viewpoints.
- In a case where the base (C) contains water and alcohols, the mixing ratio between water and alcohols can be arbitrarily adjusted in consideration of antifreeze properties and inflammability. The mass ratio between water and alcohols in the base is preferably 20:80 to 90:10 (water:alcohols), and more preferably 40:60 to 75:25 from the viewpoint of avoiding generation of a flash point.
- The kinematic viscosity at 25° C. of the coolant composition of the present invention is 8.5 mm2/s or more from the viewpoint of suppressing cooling loss at a low temperature, and is preferably 3000 mm2/s or less from the viewpoint of avoiding a load on a water pump and suppressing poor fuel efficiency of an internal combustion engine. From these viewpoints, the kinematic viscosity at 25° C. thereof is preferably 8.5 to 3000 mm2/s, more preferably 9 to 2000 mm2/s, and even more preferably 50 to 1000 mm2/s.
- From the viewpoint of maintaining the cooling capacity at a high temperature and preventing overheating, the kinematic viscosity at 100° C. of the coolant composition of the present invention is 2.0 mm2/s or less, preferably 0.3 to 2.0 mm2/s, and more preferably 0.4 to 1.8 mm2/s. The cooling capacity of the coolant composition can be evaluated, for example, by measuring the thermal transmittance of a radiator. The kinematic viscosity at 100° C. of the coolant of 100% water is 0.3 mm2/s.
- In the coolant of the present invention, it is possible to set the kinematic viscosity to be in the predetermined range described above by including the components described above. In a case where it is desired to increase the kinematic viscosity at 25° C., this can be achieved by a method of increasing the content of the surfactant (A), a method of adjusting the content of the alkali metal compound (A′) in a case of using the alkali metal compound (A′), a method of increasing the content of alcohols in a case where the base (C) contains the alcohols, and the like. In addition, in a case where it is desired to decrease the kinematic viscosity at 100° C., this can be achieved by a method of decreasing the content of the surfactant (A), a method of adjusting the content of the alkali metal compound (A′) in a case of using the alkali metal compound (A′), a method of decreasing the content of alcohols in a case where the base (C) contains the alcohols, and the like.
- If necessary, other additives than the components (A) to (C) described above may be mixed in the coolant composition of the present invention in a range in which the effects of the present invention are not impaired.
- For example, in order to effectively suppress the corrosion of metals used in an engine coolant path, the coolant composition of the present invention may include at least one rust inhibitor in a range in which the effects of the present invention are not impaired. Examples of the rust inhibitor include any one or a mixture of two or more of phosphoric acid and/or a salt thereof, an aliphatic carboxylic acid and/or a salt thereof, an aromatic carboxylic acid and/or a salt thereof, a triazole, a thiazole, a silicate, a nitrate, a nitrite, a borate, a molybdate, and an amine salt.
- For example, in order to prevent corrosion of metals, the coolant composition of the present invention may include at least one pH adjusting agent in a range in which the effects of the present invention are not impaired. Examples of the pH adjusting agent include any one or a mixture of two or more of sodium hydroxide, potassium hydroxide, and lithium hydroxide.
- The pH at 25° C. of the coolant composition of the present invention is preferably 6 or more and more preferably 7 or more, and is preferably 10 or less and more preferably 9 or less.
- To the coolant composition of the present invention, for example, a coloring agent, a dye, a dispersing agent, a bittering agent, or the like may be appropriately added in ranges in which the effects of the present invention are not impaired.
- The total amount of the above-mentioned other additives mixed therein is typically 10 parts by mass or less and preferably 5 parts by mass or less with respect to 100 parts by mass of the composition.
- In the present invention, a production method of the coolant composition is not particularly limited as long as the effects of the present invention can be obtained, and a typical production method of a coolant composition may be used. For example, the coolant composition can be produced through uniform stirring at a low temperature. The coolant composition of the present invention is more preferably obtained by, after mixing, heating the mixture to preferably 60° C. or higher, more preferably 80° C. or higher and preferably 100° C. or lower, stirring the resultant if necessary, dissolving the resultant, and thereafter cooling the resultant to room temperature (20° C.).
- The present invention also relates to an automotive engine concentrated coolant composition (hereinafter, also referred to as concentrated coolant composition of the present invention). The concentrated coolant composition of the present invention is a composition containing the surfactant (A) as the viscosity index improver of the coolant composition of the present invention, the rubber swelling inhibitor (B), and a solvent (C′) if necessary. The concentrated coolant composition of the present invention can be used for obtaining the coolant composition of the present invention by being diluted, for example, 2 to 10 times by mass with the base (C). The solvent (C′) is a liquid that can be used in a typical coolant composition such as water and glycols, and as specific examples thereof, the above description regarding the base (C) is cited. In addition, the solvent (C′) may be the same as or different from the base (C). The concentrated coolant composition of the present invention can suppress swelling of rubber after being diluted even in a case where the surfactant (A) as the viscosity index improver, the rubber swelling inhibitor (B), and the alkali metal compound (A′) if necessary are concentrated beforehand. Therefore, the concentrated coolant composition can be used as the coolant composition by being diluted with the base (C) immediately before being supplied to the engine. In addition, other additives can be mixed in the concentrated coolant composition of the present invention in a range in which the effects of the present invention regarding the obtained coolant composition are not impaired. As the additives, the above description regarding the coolant composition of the present invention is cited. Furthermore, the additives may also be mixed in the solvent (C′) for use.
- An embodiment of the concentrated coolant composition of the present invention may include, with respect to 100 parts by mass of the concentrated coolant composition, the following components: (A) the surfactant as the viscosity index improver: 0.1 to 99 parts by mass; (B) the rubber swelling inhibitor: 0.1 to 5 parts by mass; and (C′) the solvent: 0 to 99.8 parts by mass.
- The concentrated coolant composition of the present invention may contain the alkali metal compound (A′). The content of the alkali metal compound (A′) in the concentrated coolant composition of the present invention is, with respect to 100 parts by mass of the concentrated coolant composition, preferably 1 to 30 parts by mass, and more preferably 5 to 15 parts by mass.
- The coolant composition of the present invention can be generally used as a coolant and is preferably used as a coolant for an internal combustion engine. Accordingly, the present invention also relates to a method of operating an internal combustion engine in which the coolant composition of the present invention is used as a coolant (hereinafter, also referred to as a method of operating an internal combustion engine of the present invention). According to the method of operating an internal combustion engine of the present invention, it is possible to greatly improve the fuel efficiency effect of the internal combustion engine. The coolant composition of the present invention can also be used as a coolant for a battery stack, a fuel cell stack, or the like.
- Hereinafter, the present invention will be described in more detail using examples, but the present invention is not limited to these examples. In addition, numerical values in the formulation represent parts by mass.
- [1. Preparation of LLC]
- Materials of the formulation shown in Table 1 below were added, stirred, and mixed together, thereby producing an LLC. In Table 1, sebacic acid manufactured by Kokura Synthetic Industries, ltd. as a rust inhibitor, and caustic potash manufactured by Osaka Soda Co., Ltd. as a pH adjusting agent were used. The structure of a compound used as a rubber swelling inhibitor is shown below.
-
TABLE 1 LLC Material Mixing amount (parts by mass) Ethylene glycol 90.6 Water 1.2 Rust inhibitor 4.2 pH adjusting agent 4 - A rubber swelling inhibitor described in Tables 2-1 and 2-2 below, a polyoxyethylene alkyl ether sulfuric acid ester salt (Rc in formula (4) is a linear alkyl group having 22 carbon atoms, Rd is ethylene group, q is 4, and M is sodium) as a surfactant (A) (viscosity index improver), and water were mixed in the LLC at mixing amounts (parts by mass) described in Tables 2-1 and 2-2 so that the total amount thereof reached 100 parts by mass, thereby producing coolant compositions of Examples 1 to 6 and coolant compositions of Comparative Examples 1 to 11. There, the polyoxyethylene alkyl ether sulfuric acid ester salt was synthesized as follows.
- <Synthesis Method of Polyoxyethylene Alkyl Ether Sulfuric Acid Ester Salt>
- Using a thin-film sulfation reactor having an outer jacket, an alcohol ethoxylate (the average number of moles of ethylene oxide added was 4.0) of a higher alcohol primarily containing 22 carbon atoms (trade name: KALCOL 220-80 manufactured by Kao corporation) was caused to flow down in a thin film form at a supply rate of 5.0 L/h, and sulfur trioxide gas diluted with dry air (concentration of sulfur trioxide gas: 1.1 vol %) was added under conditions of a reactor cooling temperature of 40° C. and a supply rate of 130 L/min (molar ratio of sulfur trioxide/ethoxylate:1.00) to carry out a sulfation reaction.
- The obtained polyoxyethylene alkyl ether sulfate was neutralized by a 2.5% sodium hydroxide aqueous solution (molar ratio of sodium hydroxide/polyoxyethylene alkyl ether sulfuric acid ester: 1.10) so as to cause the concentration of polyoxyethylene ether sodium sulfate to be 23% or more and 27% or less such that polyoxyethylene alkyl ether sodium sulfate having 22 carbon atoms (the average number of moles of ethylene oxide added was 4.0) was synthesized.
- <Evaluation Tests>
- The obtained coolant compositions were subjected to the following evaluation tests.
- <1. Test of Effect on Viscosity Index>
- The kinematic viscosity at 25° C. was measured according to JIS K 2283. A case where the kinematic viscosity at 25° C. of the coolant composition was 8.5 mm2/s or higher was evaluated as good.
- <2. Measurement of Rate of Change in Rubber Volume>
- The temperature of the coolant was set to 120° C., a test piece of H-NBR rubber was immersed under an oxygen pressure of 0.1 MPa for 1000 hours, and the rate of change in the volume of the test piece after immersion was measured. A rate of change in the volume of 30% or less was evaluated as good.
- <3. Discoloration Test>
- 10 g of EPDM rubber pieces were placed per 100 g of the coolant in a screw mouth bottle and the resultant was heated at 160° C. for 24 hours. Thereafter, the color of the liquid was visually observed.
- The results are shown in Tables 2-1 and Table 2-2 below.
-
TABLE 2-1 Comparative Comparative Example 1 Example 2 Example 3 Example 4 Example 5 Example 6 Example 1 Example 2 Compo- LLC 53 53 53 53 53 53 53 53 sition Water 46.45 46 46.45 46 46.45 46 47 46.5 Viscosity Polyoxyethylene 0.5 0.5 0.5 0.5 0.5 0.5 — 0.5 index alkyl ether sulfuric improver acid ester salt Rubber Methyl 3,5- 0.05 0.5 0.025 0.25 — swelling dihydroxybenzoate inhibitor p-methoxyphenol 0.05 0.5 0.025 0.25 — t-butylhydroquinone Methyl gallate — 4-t-butylpyrocatechol 3,3′- — dithiodipropionic acid Evalu- A rate of change in the 23 6 27 6 23 7 6 63 ation volume of rubber (H-NBR) of 30% or less is good Discoloration test No No No No No No No No significant significant significant significant significant significant significant significant discolor- discolor- discolor- discolor- discolor- discolor- discolor- discolor- ation ation ation ation ation ation ation ation Kinematic viscosity ≥100 ≥100 ≥100 ≥100 ≥100 ≥100 3 ≥100 at 25° C. (mm2/s) -
TABLE 2-2 Compar- Compar- Compar- Compar- Compar- Compar- Compar- Compar- Compar- ative ative ative ative ative ative ative ative ative Example Example Example Example Example Example Example Example Example 3 4 5 6 7 8 9 10 11 Compo- LLC 53 53 53 53 53 53 53 53 53 sition Water 45.5 46.48 45.5 46.48 46 46 46.45 46.4 46 Viscosity Polyoxyethylene 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5 index alkyl ether sulfuric improver acid ester salt Rubber Methyl 3,5- 1 0.02 swelling dihydroxybenzoate inhibitor p-methoxyphenol 1 0.02 t-butylhydroquinone 0.5 Methyl gallate 0.5 0.05 4-t- 0.1 butylpyrocatechol 3,3′- 0.5 dithiodipropionic acid Evalu- A rate of change in the 5 37 5 34 8 8 25 23 55 ation volume of rubber (H-NBR) of 30% or less is good Discoloration test Black- No Black- No Black- Black- Black- Black- No ened significant ened significant ened ened ened ened significant discolor- discolor- discolor- ation ation ation Kinematic viscosity ≥100 ≥100 ≥100 ≥100 ≥100 ≥100 ≥100 ≥100 ≥100 at 25° C. (mm2/s) - From Tables 2-1 and 2-2, it can be seen that the coolants of Examples 1 to 6 in which the compound (p-methoxyphenol) expressed by the formula (1) and/or the compound (methyl 3,5-dihydroxybenzoate) expressed by the formula (2) was contained in a specific amount had a desired kinematic viscosity and could suppress swelling of rubber and discoloration of the coolant.
- The coolant composition of the present invention is suitably used for cooling an internal combustion engine, particularly an automotive engine, an inverter, a battery, and the like.
Claims (11)
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| JP2016-125972 | 2016-06-24 | ||
| JP2016125972A JP6430999B2 (en) | 2016-06-24 | 2016-06-24 | Automotive engine coolant composition, automotive engine concentrated coolant composition, and internal combustion engine operating method |
| PCT/IB2017/000749 WO2017221060A1 (en) | 2016-06-24 | 2017-06-20 | Automotive engine coolant composition, automotive engine concentrated coolant composition, and method of operating internal combustion engine |
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| US20190194516A1 true US20190194516A1 (en) | 2019-06-27 |
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| US (1) | US10883031B2 (en) |
| JP (1) | JP6430999B2 (en) |
| CN (1) | CN109689834B (en) |
| DE (1) | DE112017003138T8 (en) |
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20190309200A1 (en) * | 2018-04-04 | 2019-10-10 | Clement R. Hipple | Head gasket correction coagulation |
| US10913883B2 (en) * | 2016-04-04 | 2021-02-09 | Toyota Jidosha Kabushiki Kaisha | Coolant composition and method of operating internal combustion engine using the same |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
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| JP6638838B2 (en) | 2018-03-30 | 2020-01-29 | ダイキン工業株式会社 | Molded article with surface in contact with coolant |
| CN114453142B (en) * | 2022-01-14 | 2023-11-24 | 张志� | Lead-zinc sulfide mineral flotation carbon inhibitor and process |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4610222A (en) * | 1984-07-23 | 1986-09-09 | Union Carbide Corporation | Cooling system using an oil-in-alcohol containing consolute antifreeze composition |
| US20040069342A1 (en) * | 2001-01-23 | 2004-04-15 | Martin Hellsten | Drag reduction of a heat-distributing water-based liquid contaning large amounts of anti-freeze |
| US7001531B2 (en) * | 2001-08-24 | 2006-02-21 | Dober Chemical Corp. | Sustained release coolant additive composition |
| US20070200088A1 (en) * | 2006-02-10 | 2007-08-30 | Ann Wehner | Heat transfer compositions comprising renewably-based biodegradable 1,3-propanediol |
| US7387748B2 (en) * | 2002-12-02 | 2008-06-17 | Texaco Inc. | Antifreeze coolant composition for high temperature applications |
Family Cites Families (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB961409A (en) | 1961-05-24 | 1964-06-24 | United States Borax Chem | Corrosion inhibitor compositions |
| JPS594278B2 (en) | 1976-06-18 | 1984-01-28 | 株式会社日立製作所 | Collision avoidance method for multi-arm robots |
| JPS58133382A (en) | 1982-02-03 | 1983-08-09 | Katayama Chem Works Co Ltd | Corrosion inhibitor for calcium chloride brine |
| JPS594278A (en) | 1982-06-29 | 1984-01-11 | Matsushita Electric Ind Co Ltd | Blooming preventing device |
| JPH0251988A (en) | 1988-08-12 | 1990-02-21 | Pioneer Electron Corp | System for transmitting color video signal |
| RU2196797C1 (en) | 2001-08-30 | 2003-01-20 | Белокурова Ирина Николаевна | Superconcentrate for preparing antifreezes and heat carriers |
| WO2005054398A1 (en) | 2003-12-01 | 2005-06-16 | Shishiai-Kabushikigaisha | Coolant composition |
| JP5379990B2 (en) * | 2008-03-31 | 2013-12-25 | シーシーアイ株式会社 | Antifreeze / coolant composition |
| US8771542B2 (en) * | 2008-07-11 | 2014-07-08 | Prestone Products Corporation | Heat transfer fluid, additive package, system and method |
| CA2732343C (en) * | 2008-07-29 | 2017-05-09 | The Board Of Regents Of The University Of Texas System | Selective inhibition of polyglutamine protein expression |
| CN101580702B (en) * | 2009-05-31 | 2011-04-13 | 江苏盈天化学有限公司 | Antifreezing fluid |
| CN102108288A (en) * | 2009-12-28 | 2011-06-29 | 宋晓东 | Novel automobile antifreeze |
| CN102336991A (en) * | 2011-07-19 | 2012-02-01 | 中橡集团曙光橡胶工业研究设计院 | Methanol gasoline-resistant rubber material |
| KR101420746B1 (en) * | 2011-09-23 | 2014-07-21 | 극동제연공업 주식회사 | Cooling Liquid Composition for Fuel-Cell Comprising Hydroquinone or Quinoline |
| CN102492495A (en) * | 2011-11-25 | 2012-06-13 | 江苏玖尚燃油发展有限公司 | Methanol gasoline for vehicles |
| US9212597B2 (en) | 2012-06-08 | 2015-12-15 | Toyota Jidosha Kabushiki Kaisha | Coolant composition for internal combustion engine and method for operating internal combustion engine |
| JP6045956B2 (en) * | 2013-03-28 | 2016-12-14 | シーシーアイ株式会社 | Coolant composition |
| US9540558B2 (en) * | 2013-06-12 | 2017-01-10 | Ashland Licensing And Intellectual Property, Llc | Extended operation engine coolant composition |
| CN104449580B (en) * | 2013-09-24 | 2018-01-26 | 中化蓝天集团有限公司 | A kind of composition containing HFC 161 and stabilizer |
| JP2015074669A (en) | 2013-10-07 | 2015-04-20 | シーシーアイ株式会社 | Coolant composition |
| CN104673253A (en) * | 2013-12-03 | 2015-06-03 | 青岛惠城石化科技有限公司 | Research on components of novel automotive anti-freeze fluid |
| CN103965976A (en) * | 2014-03-25 | 2014-08-06 | 宁夏宝塔石化科技实业发展有限公司 | Technological formula of high-proportion methanol gasoline compound additive |
| CN104087257A (en) * | 2014-07-26 | 2014-10-08 | 司徒建辉 | Coolant composition |
| CN105482857A (en) * | 2014-09-17 | 2016-04-13 | 天津开发区信达化工技术发展有限公司 | Methanol gasoline with stable performance |
| CN104497993B (en) * | 2014-12-09 | 2017-10-24 | 广东三和化工科技有限公司 | A kind of anti-icing fluid and preparation method thereof |
| JP6154371B2 (en) | 2014-12-26 | 2017-06-28 | トヨタ自動車株式会社 | Coolant composition and method for operating internal combustion engine using the same |
| CN105368547A (en) * | 2015-11-11 | 2016-03-02 | 安徽孟凌精密电子有限公司 | Cooling solution for machining |
| JP6441837B2 (en) | 2016-01-28 | 2018-12-19 | トヨタ自動車株式会社 | Automotive engine coolant composition and automotive engine concentrated coolant composition |
-
2016
- 2016-06-24 JP JP2016125972A patent/JP6430999B2/en active Active
-
2017
- 2017-06-20 US US16/311,986 patent/US10883031B2/en not_active Expired - Fee Related
- 2017-06-20 WO PCT/IB2017/000749 patent/WO2017221060A1/en not_active Ceased
- 2017-06-20 CN CN201780038342.4A patent/CN109689834B/en not_active Expired - Fee Related
- 2017-06-20 DE DE112017003138.9T patent/DE112017003138T8/en not_active Ceased
- 2017-06-20 TW TW106120605A patent/TW201802226A/en unknown
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4610222A (en) * | 1984-07-23 | 1986-09-09 | Union Carbide Corporation | Cooling system using an oil-in-alcohol containing consolute antifreeze composition |
| US20040069342A1 (en) * | 2001-01-23 | 2004-04-15 | Martin Hellsten | Drag reduction of a heat-distributing water-based liquid contaning large amounts of anti-freeze |
| US7001531B2 (en) * | 2001-08-24 | 2006-02-21 | Dober Chemical Corp. | Sustained release coolant additive composition |
| US7387748B2 (en) * | 2002-12-02 | 2008-06-17 | Texaco Inc. | Antifreeze coolant composition for high temperature applications |
| US20070200088A1 (en) * | 2006-02-10 | 2007-08-30 | Ann Wehner | Heat transfer compositions comprising renewably-based biodegradable 1,3-propanediol |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10913883B2 (en) * | 2016-04-04 | 2021-02-09 | Toyota Jidosha Kabushiki Kaisha | Coolant composition and method of operating internal combustion engine using the same |
| US20190309200A1 (en) * | 2018-04-04 | 2019-10-10 | Clement R. Hipple | Head gasket correction coagulation |
| US10876023B2 (en) * | 2018-04-04 | 2020-12-29 | Clement R. Hipple | Head gasket correction coagulation |
Also Published As
| Publication number | Publication date |
|---|---|
| DE112017003138T8 (en) | 2019-05-09 |
| CN109689834A (en) | 2019-04-26 |
| JP2017226805A (en) | 2017-12-28 |
| DE112017003138T5 (en) | 2019-03-14 |
| JP6430999B2 (en) | 2018-11-28 |
| US10883031B2 (en) | 2021-01-05 |
| TW201802226A (en) | 2018-01-16 |
| WO2017221060A1 (en) | 2017-12-28 |
| WO2017221060A9 (en) | 2019-03-07 |
| CN109689834B (en) | 2021-04-16 |
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